Connecting...

W1siziisijiwmtcvmdmvmtyvmtavndqvmjyvndq1l2jhbm5lci1kzwzhdwx0icgyks5qcgcixsxbinailcj0ahvtyiisijiwmdb4mjawiyjdxq

QA Pharmacist, Pharmaceuticals

Vacancy Title: QA Pharmacist, Pharmaceuticals
Contract Type: Permanent
Location: Bolton, Greater Manchester
Industry:
Salary: Negotiable
REF: J902024_1566220266
Contact Name: Tom Hammond
Contact Email: tom.hammond@russell-taylor.co.uk
Vacancy Published: 27 days ago

Vacancy Description

QA/ Quality Assurance Specialist - Pharmaceutical

Location: Bolton

Type: Permanent (Mon -Friday)

Salary: CIRCA £25,000 plus additional benefits

Our Client, a leading Pharmaceutical Company is growing and are looking to recruit for a QA specialist to work at their modern manufacturing facility; the successful Candidate will play a vital role in the growth and development of the QA function and QMS.

This role is an ideal opportunity for someone working in a GLP - GMP QA Lab based role wanting to move into a full - time QA position.

The Role:

  • Providing a quality assurance compliance service to the Operations team to meet GMP and pharmaceutical licence standards.
  • Generating and maintaining technical agreements
  • Maintaining supplier assurance documentation for APIs and excipients including supply chain maps, excipient risk assessments and accreditation certificates.
  • Investigate Customer Complaints
  • Performing internal audits in line with company schedule
  • Supervising the generation of the export documentation
  • Preparing annual PQR's
  • Performing quality checks on batch and QC documentation
  • Writing SOP's, specifications, protocols and reports as required
  • Completing all documentation accurately & to meet deadlines
  • Working to SOPs and GMP standards at all times
  • Keeping your area of work clean and tidy, adhering to set housekeeping standards to minimise contamination.
  • Working as part of the overall quality team, being flexible and adaptable and assisting other team members as required to ensure targets are met.
  • Communicating with the team and inform the Quality Manager of any difficulties at any time throughout the day.
  • To work towards continuous improvement.
  • To follow Company rules as specified in the Company Handbook.
  • To adhere to all Health & Safety practices

The Person:

  • Will hold a Degree in a relevant/ scientific discipline
  • Will have experience in CAPA within a GMP setting
  • Will have had exposure to audits and complaints handling
  • Strong interpersonal skills

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k