Covalent Laboratories hiring multiple pharma roles. B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma
- Company Overview
- Job Role & Responsibilities
- Production – Documentation
- Production
- EHS (Safety)
- AR&D (Analytical Research & Development)
- Quality Assurance
- QC – Instrumentation
- QC – Validation
- Eligibility / Qualifications
- Required Education
- Experience Criteria (Department-wise)
- Location & Salary
- Employee Benefits
- Application Process
- Walk-In Interview Dates
- Interview Venue
- Registration Link
- Contact Details
- Frequently Asked Questions (FAQs)
- Who can attend the Covalent Laboratories walk-in interview?
- Are freshers eligible for these pharma jobs?
- Is prior pharma experience mandatory?
- Is online registration mandatory?
- What benefits are offered by Covalent Laboratories?
B.Sc / M.Pharm Walk-In Jobs at Covalent Labs Sangareddy
Covalent Laboratories hiring multiple pharma roles. B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma. Walk-in at Sangareddy.
Covalent Laboratories has announced large-scale walk-in interviews for multiple pharmaceutical job openings at its manufacturing and R&D facility in Sangareddy, Telangana. This hiring drive targets freshers as well as experienced professionals across production, quality, safety, and research functions. Candidates holding B.Sc, M.Sc, B.Pharmacy, M.Pharmacy, and Diploma qualifications can directly attend the interviews on the scheduled dates and explore stable, growth-oriented careers in a regulated pharmaceutical environment.
This walk-in opportunity is especially valuable for candidates seeking pharma jobs with competitive benefits, hands-on exposure, and long-term career progression in an API-focused organization. With hiring across multiple departments and experience ranges from 0 to 8 years, Covalent Laboratories is positioning this drive as one of the most accessible and high-intent pharma recruitment events in early 2026.
Company Overview
Covalent Laboratories is a well-established pharmaceutical company specializing in the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and intermediates for global markets. The organization operates with a strong compliance-driven culture aligned with international regulatory standards, making it a trusted partner for regulated market supplies.
Over the years, Covalent Laboratories has built its reputation on process excellence, quality assurance, and employee safety. The Sangareddy facility is equipped with modern production blocks, advanced analytical laboratories, and structured EHS systems. Professionals working at Covalent gain exposure to real-world regulatory practices, documentation systems, and cross-functional collaboration, which significantly strengthens long-term employability in the pharmaceutical industry.
By investing in training, infrastructure, and employee welfare, Covalent Laboratories continues to attract skilled pharma professionals looking for stability, ethical practices, and meaningful contributions to healthcare supply chains.
Job Role & Responsibilities
This walk-in hiring drive covers multiple departments, each offering role-specific responsibilities and learning exposure. Selected candidates will be placed based on qualification, experience, and interview performance.
Production – Documentation
- Preparation, review, and control of batch manufacturing records
- Ensuring real-time documentation in compliance with GMP standards
- Coordination with production and quality teams for record accuracy
- Handling deviation, change control, and SOP documentation
Production
- Execution of API manufacturing operations as per approved procedures
- Operation of reactors, centrifuges, dryers, and related equipment
- Monitoring critical process parameters and maintaining batch consistency
- Adherence to safety, quality, and productivity standards
EHS (Safety)
- Implementation and monitoring of Environment, Health, and Safety systems
- Conducting safety audits, risk assessments, and incident investigations
- Training employees on safety protocols and emergency response
- Ensuring compliance with statutory and environmental regulations
AR&D (Analytical Research & Development)
- Method development and validation for raw materials and intermediates
- Analytical testing using HPLC, GC, UV, and wet chemistry techniques
- Documentation of analytical data for development and transfer activities
- Supporting scale-up and regulatory filing requirements
Quality Assurance
- Review and approval of batch records, SOPs, and validation documents
- Handling deviations, OOS, OOT, and CAPA activities
- Ensuring GMP compliance across production and quality functions
- Supporting internal and external regulatory audits
QC – Instrumentation
- Operation and maintenance of analytical instruments such as HPLC and GC
- Calibration and performance verification of laboratory equipment
- Troubleshooting instrument-related issues
- Ensuring data integrity and compliance with laboratory SOPs
QC – Validation
- Analytical method validation and verification activities
- Preparation of validation protocols and reports
- Review of validation data for compliance and accuracy
- Supporting regulatory submissions and inspections
Eligibility / Qualifications
Covalent Laboratories is hiring candidates from diverse academic backgrounds to support its expanding operations.
Required Education
B.Sc, M.Sc, B.Pharmacy, M.Pharmacy, Diploma (Chemical, Pharmacy, or relevant discipline)
Experience Criteria (Department-wise)
- Production – Documentation: 0–2 Years
- Production: 0–6 Years
- EHS (Safety): 4–6 Years
- AR&D: 0–4 Years
- Quality Assurance: 2–8 Years
- QC – Instrumentation: 2–6 Years
- QC – Validation: 2–6 Years
Freshers with strong academic knowledge and basic GMP awareness are encouraged to attend for entry-level roles.
Location & Salary
- Interview & Job Location: Gundla Machnoor, Sangareddy, Telangana
- Salary: Industry-competitive and based on qualification, experience, and interview performance
In addition to salary, Covalent Laboratories offers attractive employee benefits that improve overall take-home value and job satisfaction.
Employee Benefits
- Subsidized canteen facility
- Attendance bonus
- Free transportation from designated routes
- Safe and structured working environment
These benefits make the opportunity especially appealing for candidates seeking stable pharmaceutical jobs with long-term security.
Application Process
This recruitment is being conducted through direct walk-in interviews and online pre-registration.
Walk-In Interview Dates
- 24 January 2026
- 27 January 2026
Interview Venue
Covalent Laboratories, Gundla Machnoor, Sangareddy, Telangana
Registration Link
Candidates are encouraged to register in advance using the official Google Form to streamline the interview process:
https://docs.google.com/forms/d/e/1FAIpQLSd9iUYVDHqUXxuTACQ9TGWgumQcIw2VmVPZ_t5IxSCaDqYRmA/viewform
Contact Details
- Phone: 9100132004
- Email: hr@covalentlab.com
Candidates should carry an updated resume, educational certificates, and relevant experience documents.
Frequently Asked Questions (FAQs)
Who can attend the Covalent Laboratories walk-in interview?
Candidates with B.Sc, M.Sc, B.Pharmacy, M.Pharmacy, or Diploma qualifications can attend, subject to experience requirements.
Are freshers eligible for these pharma jobs?
Yes. Selected departments such as Production, Documentation, and AR&D accept freshers.
Is prior pharma experience mandatory?
Not for all roles. Experience requirements vary by department.
Is online registration mandatory?
Registration is recommended but walk-in candidates are also accepted.
What benefits are offered by Covalent Laboratories?
Subsidized canteen, attendance bonus, and free transportation are provided.
| Company | Covalent Laboratories |
|---|---|
| Vacancies | Production – Documentation, Production, EHS (Safety), AR&D, Quality Assurance, QC – Instrumentation, QC – Validation |
| Required Education | B.Sc, M.Sc, B.Pharmacy, M.Pharmacy, Diploma |
| Experience | 0 to 8 Years |
To apply for this job please visit docs.google.com.
