Total 4 job vacancies by SRG

Job Title: QC Analyst Level 1 - Synergy

Location: Ware, UK

Salary: £27,000 - 28,000 p/a

contract: 12 month FTC

Are you a chemistry graduate looking for your first role in industry? Or do you already have a background in an industrial chemistry lab but would like to develop your skills further in a GMP environment?

SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst - Level 1

Synergy, part of SRG, offer a range of scientific solutions to different Clients in the Life Sciences sector. We can offer a competitive salary, a range of excellent benefits and access to training & development opportunities within the role.

Responsibilities:

• Performs analysis of samples and supports technical investigations/ monitoring, using a range of analytical techniques related to the testing of oral solid dose medicines including HPLC for assay and impurities, dissolution, homogeneity, content of uniformity, pharmacopoeia and physical property tests
• Prepares and checks analytical data accurately according to company, customer and regulatory requirements
• Assesses the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria
• Undertakes analysis as required to support process investigations or as part of process qualification and validation exercises.
• Is responsible for assigned items of Laboratory equipment or 5S standards.
• Responsible for the safety of self and others within the Laboratory

Requirements:

• Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent.
• Experienced in QC testing of oral solid dose medicines including HPLC for assay and impurities, dissolution, homogeneity, content of uniformity, pharmacopoeia and physical property tests.
• Is proficient in the use of numerous Laboratory instruments, software packages and other analytical techniques (e.g. Empower 3).
• Is proficient in problem solving and may have expertise in troubleshooting analytical equipment.
• GMP experience would be desirable but not essential.

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

Job Title: QC Analyst- Respiratory

Location: Ware, UK

Salary: £27-28.5K p/a

Contract: 12 month FTC

SRG is currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst.

Core responsibilities:

Support the Quality Assurance Department in ensuring that all aspects of the manufacture of medicinal products are performed in controlled manner and meet commitments to international regulatory bodies as well as the requirements of current Good Manufacturing Practice. The laboratory teams working as part of the Site Value Streams will assure that manufactured products are compliant and fit for purpose.

Principal accountabilities:

Operational:

• Performs analysis of samples and supports technical investigations/ monitoring, using a range of analytical techniques related to the testing of finish drug products including HPLC, for assay and impurities, NGI, AED, BCU and method troubleshooting.
• Prepares and checks analytical data accurately according to company, customer and regulatory requirements.
• Assesses the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria.
• Undertakes analysis as required to support process investigations or as part of process qualification and validation exercises.
• Is responsible for assigned items of Laboratory equipment or 5S standards.
• Responsible for the safety of self and others within the Laboratory.

Customer

• Analyses samples according to pre-defined test methods, specifications or Pharmacopoeia. Ensures analytical records follow ALCOA principles (attributable, legible, contemporaneously recorded, original and accurate)

Compliance

• Responsible for ensuring that Laboratory work areas maintain high standards of housekeeping and meet requirements such as 5S.
• Responsible for maintenance and calibration of Laboratory equipment as assigned by Laboratory Team Leader.
• Responsible for ensuring equipment used is calibrated, validated and fit for use. Deficiencies are resolved promptly in consultation with the responsible person or expert user.
• Analysis is undertaken safely and compliantly, meeting all required standards of EHS legislation and GMP, such as COSHH, Risk Assessments and DSE.
• Responsible for documenting and communicating Laboratory issues, such as safety, compliance and analytical issues giving rise to invalid data.
• Ensures sample solutions, standards and test media are used within expiry dates, or re-evaluated as appropriate
• Has awareness of change control processes and need to control changes.

People

• Takes responsibility for own training and development. Maintains up to date training records, as well as performance and development plans.
• Provides training in areas of expertise, such as the use of analytical equipment to fellow Analysts.
• Proactively provides feedback on the quality and effectiveness of training as it is received.
• Maintains analytical knowledge and access to systems ensuring they are up to date for all relevant equipment and techniques and seeks refresher training as required.

New Products

• May participate in method transfers and new product introduction exercises, for example, trialing new technology and methodology, providing feedback to Laboratory Team Leader and other staff.

Qualification and Experience:

• Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, with up to 1- or 2-years practical work experience.
• Experienced in QC testing of finish drug products including HPLC for assay and impurities.
• Is proficient in the use of numerous Laboratory instruments, software packages and other analytical techniques (E.g. Empower 3).
• Is proficient in problem solving and may have expertise in troubleshooting analytical equipment.
• Is competent in application of statistical and mathematical tools and formulae.
• Understands purpose of all techniques applicable to dosage form
• Is aware of relevant national/international Pharmaceutical regulatory authorities.

IT

• Competent in the use of corporate IT systems.
• Is computer literate and competent in the use of Microsoft packages.

Other:

• Effective verbal and written communication skills.
• Enthusiasm to work in a laboratory-based role.

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

Job Title: QC Analyst- Micronised Lab

Location: Ware, UK

Salary: £27-28.5K p/a

Contract: 12 month FTC

SRG is currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst.

Core responsibilities:

Support the Quality Assurance Department in ensuring that all aspects of the manufacture of medicinal products are performed in controlled manner and meet commitments to international regulatory bodies as well as the requirements of current Good Manufacturing Practice. The laboratory teams working as part of the Site Value Streams will assure that manufactured products are compliant and fit for purpose.

Principal accountabilities:

• Performs analysis of samples and supports technical investigations/ monitoring, using a range of analytical techniques related to the testing of micronised API including Particle Size Analysis (PSA) and HPLC for assay and impurities.
• Prepares and checks analytical data accurately according to company, customer and regulatory requirements.
• Assesses the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria.
• Undertakes analysis as required to support process investigations or as part of process qualification and validation exercises.
• Is responsible for assigned items of Laboratory equipment or 5S standards.
• Responsible for the safety of self and others within the Laboratory.

• Analyses samples according to pre-defined test methods, specifications or Pharmacopoeia. Ensures analytical records follow ALCOA principles (attributable, legible, contemporaneously recorded, original and accurate)

• Responsible for ensuring that Laboratory work areas maintain high standards of housekeeping and meet requirements such as 5S.
• Responsible for maintenance and calibration of Laboratory equipment as assigned by Laboratory Team Leader.
• Responsible for ensuring equipment used is calibrated, validated and fit for use. Deficiencies are resolved promptly in consultation with the responsible person or expert user.
• Analysis is undertaken safely and compliantly, meeting all required standards of EHS legislation and GMP, such as COSHH, Risk Assessments and DSE.
• Responsible for documenting and communicating Laboratory issues, such as safety, compliance and analytical issues giving rise to invalid data.
• Ensures sample solutions, standards and test media are used within expiry dates, or re-evaluated as appropriat

Qualification and Experience:

• Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, with up to 1- or 2-years practical work experience.
• Experienced in QC testing of micronised API including Particle Size Analysis (PSA) wet and dry technics on MS 2000, MS3000 and Sympatec Helos equipment and HPLC for assay and impurities.
• Is proficient in the use of numerous Laboratory instruments, software packages and other analytical techniques (e.g. Empower 3).
• Is proficient in problem solving and may have expertise in troubleshooting analytical equipment.
• Is competent in application of statistical and mathematical tools and formulae.
• Understands purpose of all techniques applicable to dosage form
• Is aware of relevant national/international Pharmaceutical regulatory authorities.

• Competent in the use of corporate IT systems.
• Is computer literate and competent in the use of Microsoft packages.

• Effective verbal and written communication skills.
• Enthusiasm to work in a laboratory-based role.

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

Job Title: Quality Manager - Global Pharmaceutical Company

Location: Ware, UK

Contract: 6 months

SRG are working with a global pharmaceutical company to help them find a Quality Manager to join their team. This is an exciting opportunity for an enthusiastic individual who has experience in a quality based role with relevant industrial experience.

This is a great opportunity where you will deal with various situations, which you will need to provide solutions, so good problem solving skills are a must. Within QA you will be presented with issues and business proposals which you will be asked your advice to ensure quality and the patient is not affected while allowing us to grow and develop as a competitive business. You will work cross functionally with different teams, gaining experience of providing key project management direction, pilot plant systems, analytical systems, medical devices, utilities and facilities.

Responsibilities:

• Providing review and approval of validation lifecycle documents from a variety of QMS within the company. Provide meaningful comments to ensure compliance with regulatory expectations/requirements.
• Provide quality oversight of internal business groups and external services partners inclusive of the following quality processes:
• Change control
• Deviation investigation inclusive of CAPA.
• May support project work as a QA representative, quality program or team activities.
• Provide advice and consultancy to GSK project teams, internal business groups and external partners to reduce regulatory risk to GSK.

Requirements:

• Proven working experience in biopharma/pharmaceutical Industry related to Quality Assurance Job scope.
• Experience of validation of analytical systems, cold chain storage, secondary manufacturing equipment, utilities and infrastructure. Computer validation if possible for networked systems and corporate facing applications.
• Ability to manage workload prioritisation in a fast paced changing environment.
• Excellent organisational skills
• Strong interpersonal skills.
• Strong written and verbal communication skills.
• A good team player and able to work independently.
• Experience with key Quality activities (i.e. Deviations Change Controls)

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