Validation Specialist (Livingston, Scotland)

  • Position: Full time
  • Open Date: Jan 22, 2021 11:53 AM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and various vaccines in development including unique vaccines against Lyme disease, chikungunya and COVID-19.

Valneva have a number of opportunities for Individuals with previous validation experience for our newly built manufacturing premises in Livingston.

Job Summary 

We are actively recruiting for Validation Specialists to assist with the definition and performance of operational validation activities that ensure that validation activities are in compliance with EU/FDA regulatory requirements and applicable guidelines.

Perform, witness and provide support and advice for required validations and qualifications on site. Acting as subject matter expert in regulatory inspections as appropriate based on involvement within the validation or project activities.

You will be responsible for:

  • Reporting to the Head of Validation, assist in the operational validation activities, including physically performing Equipment and Facility Qualifications.
  • Identify areas of improvement for validation systems/procedures and to provide support with the implementation of such improvements.
  • Generate and complete validation documentation in accordance with relevant Standard Operating Procedures, including but not limited to:
  • Validation Plans
  • Validation Protocols
  • Validation Reports
  • Participate in project groups and set acceptance criteria and define the data requirements necessary to ensure that validation work is compliant.  To ensure that the Head of Validation and other key stakeholders are informed of validation matters which may have an adverse impact on the validation status of facilities, equipment systems, the manufacturing process on product disposition (e.g. batch/lot release decisions).
  • Investigate and report Quality Issues, escalating to management as required.
  • To compile key quality data for the validation program and to make such data available to management to drive a culture of continuous improvement that is fully compliant with current EU/FDA regulations and quality requirements and Valneva Scotland Ltd business needs.
  • To keep up to date with current guidelines and regulatory requirements in respect of internal and external quality requirements.
  • To provide and/or coordinate training in validation related procedures/concepts as appropriate to meet business needs.
  • Provide support during internal/external and third-party audits.
  • Any other reasonable duties as requested by the Head of Validation Scotland.

Education / Experience:

  • HND level or equivalent qualification in relevant subject (required).
  • Working knowledge of Equipment Qualification and/ or Facility Qualification in a biopharmaceutical or pharmaceutical GMP environment (required).
  • Working knowledge of validation principles in at least one of the following (preferred):
  • Validation of aseptic processes (including filling),
  • Validation of Computerised systems,
  • Process Validation,
  • Assay Validation,
  • Cleaning Validation.
  • Experience in regulatory inspections (preferred).

You will have:

  •  Effective communication skills across all personnel levels within the organisation and with contractors / external engineers.
  • Good Writing skills for completion of documentation and report writing.
  • Good working knowledge of Microsoft Office including Word, Excel and PowerPoint.
  • A logical approach to problem solving
  • Good organisational and effective prioritisation skills
  • Ability to operate with minimal direct supervision
Apply Now

Manufacturing Assistant – Cleanroom (Livingston, Scotland)

  • Position: Full time
  • Open Date: Jan 8, 2021 4:07 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and various vaccines in development including unique vaccines against Lyme disease, chikungunya and COVID-19.

Valneva have a number of opportunities for Individuals with previous clean-room cleaning experience for our newly built manufacturing premises in Livingston.

Job Summary

We are looking for people to appropriately carry out all cleaning activities related to production support for ourCOVID-19 Vaccine Manufacturing Programme, according to set procedures and protocols and to best cGMP work practices and quality standards.

You will be responsible for:

  • Carrying out routine cleaning of the commercial manufacturing facility (and CTM facility as required) to a defined schedule of activities
  • Ensuring housekeeping within the cleanroom suites and common areas is maintained to a high standard at all times
  • Ensuring that response cleans are completed in a timely manner and to appropriate standards
  • Processing of orders picked from stores into the cleanroom to ensure manufacturing schedule adherence and contamination control
  • Supporting our Manufacturing activities by processing return of cleanroom garments, mops and other items as required
  • Applying best cGMP work practices and techniques
  • Immediately escalating and reporting any deviations involving materials, facilities, processes or procedures to line management
  • Conducting all activities in a careful and safe manner and in full compliance with HSE requirements
  • Supporting QMS investigations and any corrective actions and improvement opportunities
  • Identifying areas for continuous improvement and escalating those to the line manager
  • Actively contributing to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team-setting
  • Participating in training of staff in areas of expertise
  • Be flexible to work shifts and out of hours work as required
  • Undertake any other duties as requested by the line manager in accordance with company requirements

You will have:

  • A meticulous approach to all cleaning and production support activities
  • Flexibility, as there may be a variance in daily schedules from time to time
  • Previous experience of cleaning in a clean room environment (although on-going training will be provided)

Additional Required Skills:

  • Excellent attention to detail
  • Ability to follow SOPs

Please Note:

As this role involves working in our cleanroom environment, you will be required to undergo a Health Screening procedure with a suitably qualified Doctor as part of our recruitment process.  We also conduct a Disclosure Scotland Check on all prospective new hires.

Apply Now

Manufacturing Scientist (Livingston, Scotland)

  • Position: Full time
  • Open Date: Dec 10, 2020 5:26 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and various vaccines in development including unique vaccines against Lyme disease, chikungunya and COVID-19.

An opportunity has arisen in Livingston for multiple Manufacturing Technicians.  Initially working on a Mon – Fri dayshift, we will extend to become a 24/7 manufacturing operation at some point in mid-2021.  We are asking your shift preferences so that we can discuss potential working patterns based on the various information provided.

Job Summary

The purpose of this role is to execute defined and trained manufacturing steps for the production of a COVID-19 vaccine according to set procedures and protocols and according to best cGMP work practices and Quality standards.

Key Responsibilities

  • Execute production steps defined by SOPs, production records and protocol for manufacture of a Covid vaccine
  • Apply best cGMP work practices and techniques
  • Conduct on-time reporting according to defined document management standards
  • Immediately escalate and report any deviations to materials, facilities, processes or procedures to the supervising team
  • Conduct all activities in the most careful and safe manner and in full compliance with HSE requirements
  • Ensure that at any time equipment, facilities and materials used in the area of responsibility comply with defined standards
  • Support change controls, investigations and CAPAs in the most diligent manner
  • Identify areas for continuous improvement and escalate those to the respective manufacturing supervisor or appropriate person
  • Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting
  • Shift work and out of hours work as may be required
  • To undertake any other duties as requested by the line manager in accordance with company requirements
  • Be accountable that the individual workspace is clean, tidy and well organised

Experience

  • Relevant degree or HNC/HND or equivalent experience
  • Experience of cell culture and aseptic technique is essential
  • Cleanroom experience
  • Experience of working within a cGMP environment
  • Experience of following SOPs within defined cGMP work practices

Competencies

  • Self-motivated individual
  • Excellent comportment in cleanroom environment
  • Good attention to detail and adherence to procedures
  • Ability to execute activities following direction
  • Experience of working in a busy team and at times, demanding environment
Apply Now

Quality Control Technician – Sample Stability (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 26, 2020 5:42 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and several vaccines in development, including unique vaccines against Lyme disease, chikungunya and COVID-19.

Do you have a background within Quality Control and thrive in getting the best out of the people you work with? If so, we’d love to hear from you! Valneva is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs, and we are currently hiring for a Quality Control Tech to join us during this unprecedented time of growth.

Responsibilities

  • Manage and co-ordinate QMS to ensure on time delivery and compliance within the QC department
  • Manage and co-ordinate the storage of QC samples including maintenance of inventory logs, execution of routine stock checks and discard of reference material
  • Manage the storage and supply of master and working cell banks and master and working virus seed banks
  • Support routine housekeeping activities in QC including cleaning of equipment and laboratory areas
  • Co-ordinate sample logistics for all testing for the release of raw materials
  • Apply best cGMP work-practices and techniques to sampling and management of testing and release of raw materials and stability samples
  • Design and implement product stability studies.
  • Co-ordinate and schedule the testing of stability samples on a weekly, monthly and annual basis to ensure all stability time points are met.
  • Co-ordinate submission of stability samples to QC, or external test houses for testing.
  • Report stability data via interim and annual reports
  • Ensure that facilities and equipment required to adequately support required stability studies and sample storage are maintained appropriately.
  • Provide cover for raw materials and shipment activities when required
  • Identify and implement areas for continuous improvement and escalate to Lab Manager
  • Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting
  • To undertake any other duties in accordance with company requirements

Job Requirements 

  • Degree in biological sciences or relevant experience
  • Knowledge of GMP guidelines and regulatory bodies
  • Experience of Quality Management Systems
  • Awareness of raw materials / stability testing
  • Knowledge of sample management / shipping / logistics

Why work for Valneva?

  • A competitive salary, rewarding benefits package and the opportunity to work on a ground breaking vaccine project
  • Real career development opportunities and a life-long career with an innovative, forward thinking vaccine specialist with family values
  • Flexible working options
Apply Now

Government and Public Affairs Manager (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 23, 2020 5:17 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and several vaccines in development, including unique vaccines against Lyme disease, chikungunya and COVID-19.

We are looking for a creative and results-driven Government and Public Affairs Manager to manage Valneva’s visibility among government decision makers, as well as the public at large and other stakeholders. Also to manage local and site events with the Site Executive/Management Team.

The Government and Public Relations Manager will be responsible for directing the Company’s policies and objectives regarding local, Scottish and UK government affairs. The incumbent will maintain relationships with government authorities and committees in order to protect and advance the Company’s interests, fielding all inquiries from government officials, including those related to the Company’s COVID-19 vaccine. The Government and Public Relations Manager will also establish corporate strategies, policies and plans that align with evolving laws, regulations and standards.

The Government and Public Relations Manager will also be responsible for overseeing the development and execution of various publicity campaigns, including on social media, ensuring that the Valneva brand is consistent and well received by a broad audience.

To be successful in this role, the Government and Public Relations Manager should be a highly articulate and excellent presenter with a deep understanding of digital media. The top candidate will be a strong communicator, capable of representing the Company effectively to both government and the public.

Responsibilities:

  • Plan and execute local publicity campaigns in collaboration with the Investor Relations and Corporate Communications team
  • Develop and maintain relationships with public institutions, media and influencers in the vaccine space
  • Continue to build the VLA brand on social media
  • Track campaign success and media coverage
  • Ensure brand consistency in all content
  • Address negative press or PR crises if they occur
  • Feed UK issues into global policy and messages

Requirements:

  • Advanced degree in Political Science, Communications, Marketing, Journalism or another relevant field
  • 10+ years’ experience in public and/or government relations
  • Expert knowledge of UK, Scottish and local government functions
  • Excellent communication skills, both written and verbal
  • Established connections with media outlets
  • Expert knowledge of social media (ideally with an experience of building a brand)
  • Creative thinking with an affinity for innovation and problem-solving

To be successful in this role, the Government and Public Relations Manager should be a highly articulate and excellent presenter with a deep understanding of digital media. The top candidate will be a strong communicator, capable of representing the Company effectively to both government and the public.

Apply Now

HR Coordinator (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 19, 2020 12:29 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers and various vaccines in development including unique vaccines against Lyme disease, chikungunya and COVID-19.

We are looking for an HR Coordinator to join our growing team in Scotland.

Job Summary  

The HR Coordinator role covers a wide remit of responsibilities supporting the HR Manager and wider HR team with day to day HR administration activities relating to the entire HR lifecycle, including but not limited to recruitment/on-boarding, HRIS maintenance, employee relations, remuneration and benefits, performance management, employee engagement, and ad-hoc HR initiatives/projects.

The HR Coordinator must have excellent communication skills, along with a proactive approach and high attention to detail. This position will support across a busy HR team and therefore the individual needs to be able to manage their time effectively in order to deal with a diverse workload and conflicting deadlines. The individual will possess the interpersonal skills necessary to build positive and constructive relationships, along with the ability to work independently in a busy environment. Due to the current program of activity with Covid Vaccine development, the workload on HR is much in demand and this role will be fast paced, with a strong delivery requirement.

Responsibilities  

  • Act as the first point of call for all general HR administration queries, including the day to day management of the HR Inbox
  • Provide both transactional and advisory support in relation to all new starter paperwork, including letters of offer, contracts of employment, and all pre-employment required documentation
  • Be responsible for the smooth induction of new employees, ensuring correct documentation has been issued upon role acceptance, and necessary arrangements have been made to attend required training and induction sessions.
  • Ensure the timely provision, return, monitoring, and recording of documentation in relation to HR lifecycle activities such as probation reviews, annual performance development reviews, exit interview forms, etc.
  • Assist with absence management ensuring absence levels are recorded and monitored in line with company policy
  • Maintain HRIS database and regularly audit to ensure compliance is met
  • Assist with payroll data entry when required
  • Assist with the delivery of new HR initiatives and ad-hoc projects
  • Maintain knowledge in relation to employment law and assist with policy updates when required
  • Any other HR administrative task as designated by the HR Manager or Director HR UK

Why work for Valneva?

  • A competitive salary, rewarding benefits package and the opportunity to work on a ground breaking vaccine project
  • Real career development opportunities and an exciting career with an innovative, forward thinking vaccine specialist with family values
  • Flexible working options

Job Requirements

  • Proven administration experience with the ability to support in a very busy, fast-paced environment
  • HR-related qualification, or working towards
  • Working understanding of human resource principles, practices, procedures, and legislation
  • HRIS experience
  • Advanced capability in Microsoft Office; in particular Excel and Word
Apply Now

QA Specialists (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 13, 2020 1:40 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on prevention against diseases with major unmet needs. Valneva’s portfolio includes two commercial vaccines for travelers: IXIARO®/JESPECT® indicated for the prevention of Japanese encephalitis and DUKORAL® indicated for the prevention of cholera and, in some countries, prevention of diarrhea caused by ETEC. The Company has various vaccines in development including unique vaccines against Lyme disease, chikungunya and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the US with over 500 employees.

These are exciting times at Valneva! As we continue to expand our business in Livingston, we are looking for a number of QA Specialists.

The Role

To assist in developing and maintaining a comprehensive quality management system to achieve inspection readiness for Japanese Encephalitis Virus Vaccine (JEV), Coronavirus Vaccine (SARS-CoV-2) and other new products as required.  Additionally, you will act as Quality Assurance support for Valneva’s distribution network.

Your responsibilities will include:

  • Developing, monitoring, improving and maintaining procedures to ensure compliance with EU/FDA Good Manufacturing Practice for the manufacture and testing of pharmaceuticals.
  • Performing activities and reviews in accordance with relevant Standard Operating Procedures, including but not limited to:
    • Risk assessments
    • Externally prepared documents
    • CAPA
    • Change requests
    • Deviations (including Quality Investigations, EME’s and OOS)
    • Complaints (customer / supplier)
    • Development Studies / Reports
    • QMS data logs
    • Room release documentation
    • Batch record review (including PPRs, PTRs, MPRs and SPRs)
    • Fill / Finish documentation
    • Product defect reporting and Quality Investigations
    • Technical and Quality Agreements
    • Validation
  • Performing batch review duties in accordance with relevant procedures, including issuing Certificates of Non-Conformance for bulk drug product and review of QC batch test folders
  • Identifying, investigating and reporting quality issues, escalating to management as required
  • Participating in cross-functional projects
  • Developing, implementing and monitoring Continuous Improvement activities
  • Providing QA coaching / guidance for cross-functional groups to ensure compliance with KPI targets including functional QA if required
  • Co-ordinating and providing training across functional groups in Quality Procedures, cGMP requirements and QA concepts
  • Trend and report batch review and QMS data
  • Providing support to management during third-party audits
  • Performing internal housekeeping, in-process visits and quality audits
  • Performing external quality audits, supporting Livingston and other Valneva sites
  • Implementing and maintaining Quality Standard Operating Procedures, as required
  • Training staff in QA related procedures and concepts as directed by line manager
  • Undertaking any other duties as requested by the line manager in accordance with company requirements

What experience will you need?

  • Educated to degree level in relevant qualification or relevant experience
  • Proven and logical approach to problem solving
  • Previous QA experience
  • Experience of working effectively in a team, influencing as appropriate
  • Experience of working within a GMP manufacturing environment
  • Knowledge / experience of the requirements for distribution of pharmaceutical products

Your key skills will include:

  • Attention to detail
  • Excellent organisational skills
  • Effective communication skills
  • Flexible and adaptable team player
Apply Now

Health & Safety Advisor (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 12, 2020 1:12 PM
  • Location: Livingston, Scotland

Do you have a background within Health and Safety and thrive in getting the best out of the people you work with? If so, we’d love to hear from you! Valneva is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs, and we are currently hiring a Health & Safety Adviser to join us during this unprecedented time of growth.

The Role

We have a wonderful opportunity for a Health & Safety Adviser to support our organisational safety strategy, overseeing H&S policies and regulations to ensure they are fully adhered to as we move into the clinical development stages of our Covid-19 vaccine. You will continually strive to ensure Valneva meets its statutory obligations in all areas pertaining to health, safety, and welfare at work.

You would be responsible for (but not limited to):

  • Assist with the delivery of Health and Safety Inductions for all new employees
  • Updating EHS databases for health and safety accident, incident and Hear Hit events
  • Maintenance of EHS records including induction and training documentation, inspection records, accident files and follow-up action points, statistical records
  • Support responsible heads of department to complete HSE Event reports and investigations
  • Assist in setting up training sessions, prepare paperwork and file paperwork when complete
  • Assist with the Tool Box Schedule for the site and present tool box talks
  • Updating statistics in relation to safe work hours, SORs, accidents, incidents,
  • Advising and supporting employees to minimise or ultimately avoid risks and hazards in the workplace
  • Support the health and safety advisor in preparation of data for inclusion in the corporate social responsibility report

Why work for Valneva?

  • A competitive salary, rewarding benefits package and the opportunity to work on a ground breaking vaccine project
  • Real career development opportunities and a life-long career with an innovative, forward thinking vaccine specialist with family values
  • Flexible working options

What we’re looking for:

The ideal HS Adviser come from a STEM background and have possess relevant health and safety experience within the biopharmaceutical manufacturing industry or other related industries and good knowledge of environmental, health and safety practices and standards. Above all, you will possess exceptional relationship and developmental skills, and will have a track record of promoting a safe working culture within your organisation

Company Info

Valneva, established in 2013, is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs. Our Company has a growing commercial business with two successful vaccines for travellers, and our focused pipeline includes; the only Lyme disease vaccine candidate in clinical development today, a single-shot chikungunya vaccine candidate and an inactivated vaccine candidate against COVID-19.

We operate differently from players in the Pharmaceutical industry as we combine the agility and flexibility typical of specialist provider with the global coverage associated with multi-national businesses.

Apply Now

Health & Safety Manager (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 5, 2020 2:00 PM
  • Location: Livingston, Scotland

Are you a forward thinker with exceptional leadership skills? Do you have a background within HS Manager and thrive in getting the best out of the people you work with? If so, we’d love to hear from you! Valneva is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs, and we are currently hiring for a Health & Safety Manager to join us during this unprecedented time of growth.

THE ROLE

We have a wonderful opportunity for a Health & Safety Manager to support our organisational safety strategy, overseeing H&S policies and regulations to ensure they are fully adhered to as we move into the clinical development stages of our Covid-19 vaccine. You will continually strive to ensure Valneva meets its statutory obligations in all areas pertaining to health, safety, and welfare at work.

YOU WOULD BE RESPONSIBLE FOR (BUT NOT LIMITED TO):

  • Working with and training all employees to manage, monitor and improve the health and safety standards in the workplace
  • Working with the Head of Facility Management to ensure requirements for; Building regulations, fire safety, electrical safety, contractors permit to work systems, Legionella and pressure systems regulations are complied with
  • Ensure that all accidents, incidents and near hits are documented, investigated and recommended improvements implemented
  • Establish a structured health and safety system in compliance with health and safety legislation
  • Keep up to date with all aspects of relevant health, safety & welfare at work legislation and communicate relevant changes to the business
  • Provide regular reports to the Human Resources Director, Executive Management Team and Senior Management Team on relevant health and safety activities

WHY WORK FOR VALNEVA?

  • A competitive salary, rewarding benefits package and the opportunity to work on a ground breaking vaccine project
  • Real career development opportunities and a life-long career with an innovative, forward thinking vaccine specialist with family values
  • Flexible working options

WHAT WE’RE LOOKING FOR

The ideal HSE Manager will come from a STEM background and have possess relevant health and safety experience within the biopharmaceutical manufacturing industry or other related industries, as well as a post graduate qualification in Health and Safety (NEBOSH Diploma, NVQ Level 5 Diploma).

Previous line management experience is advantageous. Above all, you will possess exceptional relationship and developmental skills, and will have a track record of promoting a safe working culture within your organisation

COMPANY INFO

Valneva, established in 2013, is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs. Our Company has a growing commercial business with two successful vaccines for travellers, and our focused pipeline includes: the only Lyme disease vaccine candidate in clinical development today, a single-shot chikungunya vaccine candidate and an inactivated vaccine candidate against COVID-19.

We operate differently from players in the Pharmaceutical industry as we combine the agility and flexibility typical of specialist provider with the global coverage associated with multi-national businesses.

Apply Now

Manufacturing Process Technician (Livingston, Scotland)

  • Position: Full time
  • Open Date: Nov 4, 2020 3:31 PM
  • Location: Livingston, Scotland

An opportunity has arisen in Livingston for Manufacturing Process Technicians.

JOB SUMMARY

The purpose of this role is to execute defined and trained manufacturing steps for the large-scale production of a Covid-19 vaccine candidate, according to set procedures and protocols whilst adhering to best cGMP work practices and Quality standards.

KEY RESPONSIBILITIES

  • Execute production steps defined by SOPs, production records and protocols for manufacture of our Covid-19 vaccine candidate
  • Setting up, operating and monitoring complex manufacturing equipment
  • Apply best cGMP work practices and techniques
  • Conduct on-time reporting according to defined document management standards
  • Immediately escalate and report any deviations to materials, facilities, processes or procedures to the supervising team
  • Conduct all activities in the most careful and safe manner and in full compliance with HSE requirements
  • Ensure that at any time, equipment, facilities and materials used in the area of responsibility comply with defined standards
  • Support change controls & investigations in the most diligent manner
  • Identify areas for continuous improvement and escalate those to the respective manufacturing supervisor or appropriate line manager
  • Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting
  • Choose & commit to work one of the various shift patterns on offer
  • To undertake any other duties as requested by the line manager in accordance with company requirements
  • Be accountable that the individual workspace is clean, tidy and well organised

EXPERIENCE

  • Relevant degree, HNC/HND or equivalent experience
  • Experience as a key operator on setting up and operating complex manufacturing equipment
  • Cleanroom experience
  • Experience of working within a cGMP environment
  • Experience of following SOPs within defined cGMP work practices

COMPETENCIES

  • Self-motivated individual
  • Good attention to detail and complete adherence to procedures
  • Ability to execute activities following direction
  • Excellent behaviour and demeanour in a cleanroom environment
  • Experience of working in a busy team and demanding environment

 

Apply Now