Total 6 job vacancies by SRG

Title: QA Officer (Shifts) - 8-month Contract

Location: West Yorkshire

Salary: £32,000 - £36,500

SRG are recruiting for a Quality Assurance Officer to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS.

This position will join the QA Operations team and will supporting the QMS teams & shop floor, playing a vital role in ensuring ongoing quality & compliance.

The role

As the QA Officer, you will be responsible for:

• Supporting the Deviation systems and investigations.
• Assisting with the Implementation & review of CAPAs.
• Supporting Customer Compliant investigations.
• Supporting product quality reports & Batch review activities of licensed medicines & Medical devices.
• Ensure all activities, changes to equipment and working practices are made in line with regulations and guidelines for products including licensed medicines, medical devices, cosmetics, food, and biocides.
• Ensure all improvement opportunities are in line with ISO and all manufacturing operations are defined and documented to ensure optimum performance.

Requirements:

• A degree or similar qualification or experience in a relevant subject.
• Proven professional experience in a similar QA position & systems.
• Experienced in the use of SAP, MasterControl, QPulse or other eQMS/eDMS systems.
• A keen eye for detail, with the ability to identify & resolve issues as required.
• An effective communicator, able to effectively engage with people at all levels.
• Available to work rotation / night shifts.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Senior QA Officer (Shifts)

Location: West Yorkshire

Salary: £42,000 - £49,500

SRG are recruiting for a Senior Quality Assurance Officer to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS.

This position will take on a senior role within the QA Operations team and will support colleagues in QA and the shop floor, playing a vital role in preparing & reviewing critical documentation and coordinating batch release priorities.

The role

As the Senior QA Officer, you will be responsible for:

• Supporting the Deviation systems and investigations.
• Implementing & reviewing the effectiveness of CAPAs.
• Managing the Customer Compliant systems and related investigations.
• Producing & managing product quality reports & batch certificates.
• Batch review activities of licensed medicines & Medical devices
• Quality release of cosmetic and food products.
• Ensure all activities, changes to equipment and working practices are made in line with regulations and guidelines for products including licensed medicines, medical devices, cosmetics, food, and biocides.
• Ensure all improvement opportunities are in line with ISO and all manufacturing operations are defined and documented to ensure optimum performance.

Requirements:

• A degree or similar qualification or experience in a relevant subject.
• Proven professional experience in all aspects of quality management and management systems.
• Experienced in the use of SAP, MasterControl, QPulse or other eQMS/eDMS systems.
• A keen eye for detail, with the ability to identify & resolve issues as required.
• An effective communicator, able to effectively engage with people at all levels.
• Available to work rotation / night shifts.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: QC Validation Analyst

Location: West Yorkshire

Salary: £27,500 - £29,000

SRG are working with a pharmaceuticals company who develop & manufacture novel medicines to improve the outcomes & wellbeing of patients, unable to take traditional does forms. Based in West Yorkshire, we are looking to recruit a QC Validation Analyst on a 12-month initial contract to aid the team during a key period of growth.

This would be a great opportunity to join a highly experienced team, in a cGMP environment that can also offer flexible working hours.

The Role:

As the QC Validation Analyst, you will be responsible for ensuring the quality & compliance of raw materials & finished products by performing analysis on sample relevant to the release of products.

Key responsibilities will include:

• Conducting validation activities in accordance with cGMP regulations.
• Writing & reviewing validation documents.
• Performing QC analysis of raw materials, in - process & Finished products.
• Participate in out-of-specification / failure investigations and corrective actions.
• Reviewing external testing data to ensure accuracy & regulatory compliance

The Person:

• A degree or similar qualification in Chemistry or a relevant field.
• Previous method or cleaning validation experience within a GMP environment.
• Prior experience of HPLC would be advantageous, but not essential.
• Keen eye for detail and accuracy - with the ability to understand, review and write documents & procedures.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.com to view our other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: QC Tech Transfer Scientist

Location: Leeds

Employment Type: 12 month FTC

Salary: Competitive with flexible hours and generous package

We are currently working with a global leader in medicinal manufacturing who are looking for a QC Tech Transfer Scientist to join the Tech Transfer team. As the QC Tech Transfer Scientist, you will be responsible for successfully ensuring the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of company materials and product, according to cGMP requirements.

The main duties and responsibilities will include:

• Ensuring lab cleanliness and safety standards are maintained
• Performing analytical testing of finished products using validated methods at a high RFT.
• Performing analytical testing and Micro/PET to USP, EP, BP monographs at a high RFT
• Participate in out-of-specification and failure investigations and recommend corrective actions.

Experience required:

• A degree in a relevant scientific subject with a basic understanding of cGMP.
• At least 2 years of relevant work experience is required.

Interested? Or know someone who will be?

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you are interested in this role and require more information, please contact Elliott Howells on 0161 526 1903 or email

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Assistant QC Analyst

Location: Leeds

Employment Type: Permanent

Salary: Competitive with flexible hours and generous package

We are currently working with a global leader in medicinal manufacturing who are looking for an Assistant QC Analyst to join their raw materials team. As the Assistant QC Analyst, you will be responsible for successfully ensuring the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of company materials and product, according to cGMP requirements

The main duties and responsibilities will include:

• Ensuring lab cleanliness and safety standards are maintained
• Performs analytical testing of Finished or Stability batches using validated HPLC methods
• Ability to perform physicals testing of finished products, raw materials & Components
• Ability to document all Chemistry, Micro or packaging analysis following good data documentation practice with minimal supervision

Experience required:

• A degree in a relevant scientific subject with a basic understanding of cGMP.
• Any prior experience within industrial pharmaceutical Quality Control will naturally be beneficial.

Interested? Or know someone who will be?

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you are interested in this role and require more information, please contact Elliott Howells on 0161 526 1903 or email

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job title: QC Analyst

Location: Worthing, West Sussex

Contract: 12- month FTC.

Pay rate: £14.45p/h

SRG are looking for an QC analyst to join a global pharmaceutical company based in Worthing. As a QC analyst you would be responsible for carrying out physical and chemical analytical test methods on oral, stability and sterile products., using SOPs and accurately document the results as part of the QXC process to ensure products are of satisfactory quality for market release.

This role would be perfect for anyone with analytical chemistry testing experience, either from industry or an academic lab, whether you are coming from a QC lab, or looking for your first role out of university we would like to hear from you!

Key Responsibilities will include:

• To test routine production and stability samples supplied from the site value streams and meet testing lead-time targets.
• Calibrate and maintain analytical equipment.
• Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions ect)
• To carry our OOS investigations and discuss outcomes with other team members.
• Perform validation of equipment and methods as required.
• To adhere to and help maintain the highest levels of GLP within the section and ensure training records are kept up to date.

Candidate Requirements:

• Degree or HNC in chemistry or related discipline
• Hands on experience with HPLC, UV-Vis or other analytical testing methods.
• Experience working to GMP standards would be an advantage.
• Experience with following SOPs would be an advantage.

To apply click the link or send your CV

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.