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Sekhmet Pharmaventures Walk-in Interview – Executive / Sr. Executive Roles in Production (API), QC & Engineering on 23rd–28th March 2026

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API Pharma Jobs – Sekhmet Pharmaventures is conducting a walk-in interview from 23rd to 28th March 2026 for Executive / Sr. Executive positions in Production (API), Quality Control (QC), and Engineering (Electrical) at its Optimus Drugs Unit-3 facility in Ramlingampally.

Preference given to male candidates with 2–4 years of relevant experience in regulated API manufacturing. Bring mandatory documents for immediate shortlisting.

About the Company

Sekhmet Pharmaventures operates through its associate company Optimus Drugs, a respected manufacturer of Active Pharmaceutical Ingredients (APIs) and intermediates. The company focuses on high-quality, regulatory-compliant production with modern facilities equipped for multi-step synthesis and stringent quality control.

Optimus Drugs maintains strong adherence to GMP standards and serves both domestic and export markets. The organization emphasizes safety, compliance, documentation accuracy, and technical expertise, providing a professional environment for growth in API manufacturing, analytical testing, and plant engineering.

Job Details

  • Company Name: Sekhmet Pharmaventures (Optimus Drugs Unit-3)
  • Experience: 2–4 Years
  • Qualification: B.Sc Chemistry / B.Pharmacy / M.Sc Chemistry / M.Pharmacy / B.Tech / Diploma (relevant field)
  • Location: Optimus Drugs Unit-3, Ramlingampally, Hyderabad, Telangana
  • Work Type: On-site (API Manufacturing Plant)

Job Description

Sekhmet Pharmaventures is hiring skilled male professionals for its API manufacturing operations at Optimus Drugs Unit-3. Roles demand hands-on experience in regulated API plants with strong focus on cGMP compliance, documentation, safety, and technical execution.

Executive / Sr. Executive – Production (API)

  • Department: Production
  • Market: Pharmaceuticals – API Bulk Drugs
  • Role: Executive / Sr. Executive – Production
  • Experience: 2–4 Years
  • Education/Qualification: B.Sc Chemistry / B.Pharmacy / M.Sc Chemistry / M.Pharmacy

Executive / Sr. Executive – Quality Control (QC)

  • Department: Quality Control
  • Market: Pharmaceuticals – API Bulk Drugs
  • Role: Executive / Sr. Executive – QC
  • Experience: 2–4 Years
  • Education/Qualification: B.Sc Chemistry / M.Sc Chemistry / B.Pharmacy / M.Pharmacy

Executive / Sr. Executive – Engineering (Electrical)

  • Department: Engineering
  • Market: Pharmaceuticals – API Bulk Drugs
  • Role: Executive / Sr. Executive – Engineering (Electrical)
  • Experience: 2–4 Years
  • Education/Qualification: B.Tech / Diploma (Electrical / relevant field)

Skills/Qualifications

  • Mandatory experience in regulated API manufacturing plants
  • Production: Batch execution, SOP/BMR adherence, equipment operation, coordination with QA/QC
  • QC: HPLC/GC/wet lab analysis, GLP compliance, data integrity, OOS/deviation handling
  • Engineering: Electrical system maintenance, troubleshooting, utilities, safety compliance
  • Strong documentation, cGMP awareness, and teamwork skills
  • Preference for male candidates

Key Responsibilities

  • Execute API batch manufacturing as per SOPs/BMR with process monitoring
  • Ensure cGMP compliance, safety, and accurate documentation
  • Perform RM/IP/FP analysis using HPLC, GC, and wet lab techniques
  • Maintain GLP, data integrity, and handle OOS/deviations
  • Troubleshoot and maintain electrical systems, utilities, and automation
  • Support preventive/breakdown maintenance and commissioning activities
  • Coordinate with QA/QC and ensure smooth plant operations

Benefits/Perks

  • Career growth in a reputed API manufacturing company
  • Exposure to regulated bulk drug production and quality systems
  • Opportunities for skill development in GMP/GLP and technical processes
  • Competitive compensation based on experience
  • Supportive work culture focused on safety and compliance

How to Apply

Walk-in interview is open from 23rd March to 28th March 2026 from 09:00 AM to 12:00 PM daily. Bring mandatory documents: Educational certificates, PAN & Aadhaar, appointment letter (if any), last 3 payslips (if applicable). Candidature will not be accepted without these documents.

Sekhmet Pharmaventures Walk-in Interview – Executive / Sr. Executive Roles in Production (API), QC & Engineering (Electrical) on 23rd–28th March 2026

Candidates unable to attend can email CV to hr3@sekhmetpharma.com. For more API jobs, QC openings, production roles, and pharma walk-in interviews in Hyderabad/Telangana, visit Pharma Recruiter.

Walk in early between 23rd–28th March 2026 and secure your role with Sekhmet Pharmaventures!

Walk-in Interview Details

  • Dates: 23rd March to 28th March 2026
  • Time: 09:00 AM – 12:00 PM daily
  • Venue: Optimus Drugs Unit-3, Ramlingampally, Hyderabad, Telangana
  • Contact/Email: hr3@sekhmetpharma.com

Why You Should Join

Sekhmet Pharmaventures / Optimus Drugs offers a stable, compliance-focused environment in API manufacturing with emphasis on quality, safety, and technical expertise.

Professionals benefit from hands-on experience in regulated batch operations, analytical testing, and electrical maintenance, continuous learning in GMP/GLP, career progression, and long-term job security in Hyderabad’s pharmaceutical ecosystem.

Joining the team means contributing to high-quality APIs while growing professionally in a reputed organization committed to excellence and reliability.

FAQs

Who is eligible for the Executive / Sr. Executive roles at Sekhmet Pharmaventures?

Male candidates with 2–4 years of experience in regulated API plants; qualification in B.Sc/M.Sc Chemistry, B.Pharm/M.Pharm, or B.Tech/Diploma (Electrical).

Is prior API manufacturing experience mandatory?

Yes—candidates must have relevant experience in API production, QC, or engineering in regulated plants.

Where is the walk-in venue located?

Optimus Drugs Unit-3, Ramlingampally, Hyderabad, Telangana.

What growth opportunities exist in these roles?

Strong potential for career advancement in a regulated API company with exposure to cGMP compliance, analytical techniques, and plant operations in a reputed organization.

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