Senior Quality Control Analyst
1 week ago
**Do you have production quality assurance experience?**
**Experienced in QC testing of API (Active Pharmaceutical Ingredient)?**
**Do you hold a relevant Degree in Pharmaceutical Chemistry, Analytical Chemistry?**
**Salary is up to £23,500 + Benefits DOE**
**Monday to Friday 8.30am - 5pm**
Due to the significant expansion of our client based in Sandwich, they are now recruiting for a Senior Quality Control Analyst to join and support their team.
If successful, you will be joining a team of motivated and self-driven individuals with a passion for ensuring the success of this exciting project.
To approve physical and analytical testing and report accurate results. To support the QC Manager as to co-ordination of testing carried out within the lab.
You will be recruited as a member of the Quality Team and will report directly to the QC Manager.
**Key Responsibilities for Senior Quality Control Analyst**
- Strict adherence to GMP.
- Support the Quality Assurance Manager.
- Deputise for the QA Manager when he/she is unavailable.
- Develop and oversee Validation activities such as protocols and reports.
- Lead self-inspection audits.
- Manage all process deviations and planned process changes.
- Check and authorise all completed process documentation.
- Develop and periodically review the Validation Master Plan (VMP) alongside the QA Manager.
- Undertake external audits.
- Develop Quality databases including metrics.
- Manage product recalls alongside the QA Manager.
- Ensure Quality agreements are in place to cover business relationships.
- Generate NDA’s and Technical Agreements with any 3rd parties.
- Liaise with collaborators, contracts and customers as required.
- Oversee and manage any QMS changes.
- Document coordination to ensure all SOP’s, policies and other such documents are created, formatted and stored correctly according to company procedures.
- Write, review and update SOP’s and documentation relating to job role.
- Responsible for the management and closure of Deviations, CAPA, Change Controls and OOS/OOT’s, alongside the QA Manager.
- Training new members of staff within the QA department.
- Adhere to right first-time documentation.
- Operate independently in ambiguous situation.
- Detailed understanding and interpretation of the cGMPs, quality systems and GMP processes for the R&D environment.
- Responsible for the Technical Review and Release of batches.
- Responsible for the safety of self and others within the Laboratory
**Skills and Abilities of Senior Quality Control Analyst for the role**
- Will hold relevant Batchelor of Science degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent
- Enthusiastic self-driven individual
- Excellent working knowledge of current GMP requirements
- Excellent communication and management skills
- Ability to prioritise workload in order to meet commitments
- GMP experience
- IT literate
- High level of written and verbal communication skills required for role
- Previous audit experience
**About Morgan Jones**:
- This role is being handled by Morgan Jones Recruitment & HR Consultants. We have been established as a quality recruitment business for over 18 years with a reputation for fair and equal representation. We see each applicant as an individual and willtreat you accordingly._
- To view other great opportunities please check out our website. Follow Morgan Jones on your favourite social networks - Facebook, Twitter, LinkedIn._
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