Skip to main content
Post your CV and find your next job on Indeed!

quality control inspection jobs

Sort by: -
    • This person will oversee quality control testing related to GMP release and stability as well as lifecycle improvement for methods related to raw material, in-…
    • Manage an effective internal audit and self-inspection programme.
    • Generate, analyse, and communicate key quality performance metrics.
    • View all Boots jobs - Nottingham jobs - Quality Specialist jobs in Nottingham
    • Salary Search: QMS Quality Specialist salaries in Nottingham
    • See popular questions & answers about Boots
    • Assist in the development and agree quality plans for project activity, identifying the level and frequency of inspection required to monitor quality standards…
    • You will also participate in implementing quality control standards and procedures, and performing quality control checks and inspections on projects work and…
    •  Expert understanding of quality management systems, quality planning, assurance arrangements and progressive assurance throughout construction delivery.
    • The role ensures that controlled documents, quality records and agreed quality-system workflows are maintained accurately, progressed in a timely manner and…
    • This is a varied and hands-on role combining quality inspection, document control and quality system compliance.
    • Good report writing and numeracy skills.
    • Support inspection standards, test procedures and quality documentation.
    • Act as primary quality contact for customers.
    • Analyse quality trends, KPIs and metrics.
    • Support compliance systems including calibration control, ESD protection, IQC/OQC, MRB activity and supplier quality performance.
    • Understanding of quality assurance practices.
    • Inspect products and processes against established quality standards.
    • Minimum of 2 years experience in inspection roles preferred.
    • Goods inn and customer returns Inspection.
    • Generating FAIRs and using company MRP system.
    • Demonstrable quality management or quality control experience in manufacturing.
    • Quality Control Leadership - lead the QC function across incoming goods, in-…
    • To achieve the main objective of this role, the QC will carry out various quality control related tasks such as product quality checks at various points,…
  • View similar jobs with this employer
    • Strong understanding of document control, quality records, and compliance administration.
    • Experience in compliance, document control, administrative quality, or…
    • Experience managing or leading supplier quality activities and resolving supplier-related quality issues.
    • Establish and maintain effective production quality…

People also searched:

technical
control engineer
controller
inspection engineer
inspector
instrumentation
metrology
operative
quality assurance
quality control

Job Post Details

Senior Analyst, Quality Control
Replimune, Inc.
Abingdon
Full-time

Job details

Pay information not provided
Full-time
Abingdon

Full job description

Overview:

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold and Innovative.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients.

Join us, as we reshape the future.


Job Summary:

The role is responsible for performing the routine and non-routine QC testing following Standard Operating Procedures (SOPs) and established test methods, conduct laboratory-based activities such as reagent preparation, tissue culture, equipment maintenance, sample receipt and disposal etc. It also involves other QC tasks such as maintaining sample/reagent/consumable inventory and ordering reagents, writing and updating documents, supporting transfer of new methods and supporting audits and inspections.


This position is based in our Milton Park location and typically has a 5-day on-site expectation.

Responsibilities:
  • Perform QC testing of various routine and non-routine samples according to Standard Operating Procedures (SOPs).
  • Maintain various cell lines on regular basis by revival and passaging at set intervals.
  • Perform QC sample and material receipt and maintain inventory.
  • Routine equipment maintenance and troubleshooting as required.
  • Lead introduction of new equipment and participate in validation activities.
  • Write, update or review SOPs, protocols, FORMs and update as required.
  • Participate in QC method transfers, validation, and stability activities.
  • Adhere to current Good Manufacturing Practices (cGMP) and Good Documentation practices (GDP).
  • General lab tasks such as housekeeping, inventory of supplies, order supplies etc.
  • Write deviations/CAPA/Change controls related to QC and assist with investigations related to OOS and OOT results.
  • Become a trainer in method as processes and train junior member of the team as required.
  • Assist with internal and regulatory agency audits / inspections.
  • Ensure training is kept in GMP compliant state.
Qualifications:

Education:

  • Degree in Chemistry/Biochemistry/ other related science.


Required Experience:

  • 3 years or more of laboratory-based experience working in similar environment.
  • Competent analytical skills and attention for details.
  • Understanding of GMP requirements
  • Computer literacy (including MS Word and Excel), good communication and organizational skills.
  • Ability to work independently and with others in a team


About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.


#LI-onsite
Let Employers Find YouUpload Your Resume