This website uses cookies to ensure you get the best experience on our website. By continuing to use this site, you agree to our cookie  & privacy policy.Accept

checked This is a sample alert

Consultant – Quality Control (GLP/GMP)

  • Full Time
  • On-Site - Bengaluru
  • 6 months
  • Project posted on: 2/06/2026
add_new View Project Details

Consultant – Quality Control (GLP/GMP)

  • Manufacturing/Operations
  • Quality assurance

On-Site - Bengaluru

Full Time

6 months

 2/06/2026

Assignment Details

Our client, A leading Biotechnology company is looking to engage with consultant who can deliver the following responsibilities: 

 

  • Adherence to cGMP (Current Good Manufacturing Practice) and cGLP (Current Good Laboratory Practice).
  • To collect samples and to carry out all tests and to issue test reports as per documented procedures.
  • In process, Finished product, validation, stability samples inspection, testing and reviewing.
  • Corrective and preventive actions as and where applicable
  • Preparation / Review and maintenance of Quality of the records.
  • Preparation /Review of product specifications and analytical Record.
  • Preparation and review of certificate of analysis.
  • Training of personnel.
  • Issue and review of log sheets/Annexures/Raw data books/Checklist/log sheets for record times.
  • Handling of SAP related activities like Creation of Inspection plan, uploading of results.
  • Handling and Investigation of OOS, OOT, OOC, Deviation and Incidents.
  • Product Traceability, Visual inspection and Destruction of Reserve samples.
  • Qualification and requalification of Analytical instruments/Cooling Chambers/Rooms.
  • Preparation and Review of Analytical method validation, Method transfer and temperature mapping protocols and reports.

Skills Required

Qualification:

 

  • Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, Biotechnology, Life Sciences, or a related scientific discipline.
  • Minimum 5–8 years of experience in Quality Control, Analytical Laboratory, or Quality Assurance functions within the pharmaceutical, medical device, or regulated manufacturing industry.
  • Strong knowledge of cGMP, cGLP, GDP, and applicable regulatory requirements, including documentation and data integrity practices.
  • Hands-on experience in testing and review of raw materials, in-process samples, finished products, validation samples, and stability samples.
  • Proven experience in handling and investigating OOS, OOT, OOC, deviations, incidents, and CAPA activities.
  • Expertise in preparation, review, and maintenance of analytical records, product specifications, Certificates of Analysis (CoA), protocols, and quality documentation.
  • Experience in analytical method validation, method transfer studies, temperature mapping, and qualification/requalification of laboratory instruments and storage facilities.
  • Working knowledge of SAP Quality Management (QM) module, including inspection plan creation, result recording, and quality data management.
  • Strong analytical, problem-solving, documentation, and investigation skills with the ability to identify root causes and implement effective corrective actions.
  • Excellent communication, training, and stakeholder management skills, with the ability to work collaboratively in a cross-functional and compliance-driven environment.

About the Client

A leading Indian bio-pharmaceutical company

Industry

Pharmaceuticals

Experience Required:

5+ years

Additional Skills:

  • OOS/OOT Investigation & CAPA
  • cGMP (Current Good Manufacturing Practice) Compliance
  • Quality Documentation & Data Integrity
  • SAP QM
  • cGLP (Current Good Laboratory Practice) Compliance
  • Analytical Testing & Laboratory Operations

No of open positions:

1

Similar Freelance Projects you can apply to

View More Projects btn btn

How it works

  • 1

    Build your
    skill profile

  • 2

    Strengthen it
    with feedback

  • 3

    Determine your
    optimal fee level

  • 4

    Apply for matching
    projects

  • 5

    Get finalized

  • 6

    Stay Engaged

Build your skill prodile

Project
step1
shape_step

Request feedback from prior projects and/or work stints

shape_step

Determine your optimal fee level

  • starFeeBee helps consultants understand how to price their services.
  • starEnter your skill & location to get ranges for what similar professionals have charged on projects.
  • starUnlock more details e.g., best paying sub-skills, ranges by projects durations, by simply adding a benchmark from a orior projects.
graph_step2
shape_step

Apply for matching projects

shape_step

Get finalized!

Project
step5
shape_step

Stay Engaged!

Project
step6
shape_step

More than 3000 clients rely on Flexing It today

Frequently asked questions.

We host both full-time & part-time projects from top clients for 100+ skill categories. We also help connect experts like you with clients for short consultation calls called Flexperts

You just need to create a ‘boutique firm’ account during the registration process. The rest of the application process remains the same.

Our freelancers fee benchmarking tool, FeeBee helps our freelancers and consultants find out what their peers charged for similar projects. Built on 600K+ verified benchmarks, registered users get unlimited access to it.

As a freelancing platform, we do not provide permanent positions or full-time job to our consultant network.

Flexing It will be involved end to end right from contracts to invoicing. Once you are finalized, your payment details are transparently laid out in your contract terms with your client and our team actively liaises with the client finance team to ensure timely payments.

We do not charge any fee or commission from you. Your fee quote will be paid out to you in full as per your project contract.

planGet alerts for new project opportunities.