Team Member - QA Validation
Notify me about similar jobsWe couldn't confirm this posting on Dr. Reddy's Laboratories's site in our latest checks -- see current similar openings below.
About this opportunity
Roles & Responsibilities
Review of qualification protocols and reports of facility, area, equipment, and utilities including URS, DQ/FS, RA, SLIA, Project specific qualification plan, commissioning checklist, IQ, OQ, UTM, PQ & RQ.
Review and approval of smoke study protocol & report.
Review of VMP and their subsequent revisions.
Review of VMP re-qualification calendar for all equipment, facility, Utility etc.
Review of PMP check list/schedules and Master calibration and Facility maintenance planner etc.
Review of Audit trails, master instruments calibration certificates.
Review of logbooks for its compliance and good documentation practices.
Ensuring compliance to VMP revalidation schedule as per revalidation matrix for all equipment, facility, utility etc.
Allotment of numbering for equipment’s, area, layouts and to prepare / Update the List.
Handling and closure of quality management system which includes change controls, incidents & CAPA.
Participation in investigations that are triggered due to incidents/deviations as applicable.
Responsible for preparation, review of SOP as per requirement.
Review of BMS & EMS related documents and alarms & audit trials reports for its compliance.
Review of activity related to critical equipment breakdown notification.
Review of equipment breakdown and general maintenance notification.
Compilation and Preparation of Annual review of utilities reports.
To perform GEMBA walk in utility system i.e. HVAC, compressed air, and water system, etc.
Review of Pure steam quality reports, compressed air and nitrogen gas testing reports.
Review of documents in DocHub, e-VAL, SAP DocuSign as applicable.
Review of cleaning validation protocols and reports.
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Educational Qualification
A Bachelor's or Master's degree in Pharmacy,
Minimum Work Experience
5 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance
About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry.
We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. The World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future.
" Benefits Offered
At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
" Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions...
For more details, please visit our career website at https://careers.drreddys.com/#!/
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Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1523 comparable Quality roles across 149 biopharma companies.
Salary context
248 of 1523 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1523 comparable roles
+ 47 more countries
Seniority mix
690 of 1523 peers have a known seniority level
Therapeutic area mix
1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Currently open similar roles
This posting is closed, but here are live openings closest to it -- ranked by similarity, not by how well you'd qualify for them.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.