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Pharma Walk-In Drives: Optimus Drugs, Stallion Laboratories, Lupin, Aurenyx, Rusan & Leben

The pharmaceutical sector is hiring aggressively in November 2025. If you’re a B.Sc., M.Sc., B.Pharm, M.Pharm, B.Tech, diploma, ITI or fresh graduate looking for production, QC, QA, regulatory, instrumentation, civil, mechanical, or software roles — this consolidated guide gives you everything: clean job listings, precise role details, application emails/links, interview tips, resume/subject-line templates, likely salary ranges, and FAQs to help you get called for interviews and convert offers fast.

1) Optimus Drugs (Sekhmet Pharma) — Walk In Drive (API Production)

Positions: Graduate Trainee / Executive / Sr. Executive — Production (API)
Qualifications: B.Sc Chemistry, B.Pharmacy, B.Tech (Chemistry), M.Sc Chemistry, M.Pharmacy
Experience: 1–3 years (Immediate joiners preferred)
Dates: 17/11/2025 — 29/11/2025
Time: 09:00 AM — 03:00 PM
Venue: Optimus Drugs Unit – 3, Ramlingampally
Apply / Send CV: akhil.hari@sekhmetpharma.com; subrahmanyam.nori@sekhmetpharma.com

Role overview (API Production)

• Operate and monitor API manufacturing (reaction, filtration, drying).
• Ensure cGMP and safety compliance, area and equipment cleanliness.
• Maintain accurate BMR/BPR documentation and perform IPC checks.
• Coordinate with QA/QC for sample pulls and in-process checks.
• Report deviations and support continuous improvement initiatives.

What they look for

• Hands-on experience with batch manufacturing, reactor ops, filtration/drying cycles.
• Strong documentation discipline (BMR/BPR).
• Basic knowledge of IPCs and sample handling.
• Team players who can follow SOPs and maintain GMP standards.

Interview preparation tips

• Be ready to discuss 1–2 production batches you handled: your role, outcome, any challenges and corrective actions.
• Bring copies of BMR/BPR samples (if permitted) or describe the documentation workflow you followed.
• Emphasize safety and cGMP examples.

2) Stallion Laboratories — Multiple Positions

Departments Hiring: Production, QC, QA, ADL, PPMC, IT
Qualifications: ITI/Diploma up to M.Sc/M.Pharm/B.Pharm, B.Com/M.Com
Experience: 0–12 years (various roles)
Apply / Send CV: Darshan.mistry@stallionlabs.com
Location: Unit-II, Bavla (Ahmedabad) — USFDA & MHRA approved formulation unit

Roles & required skills (high-level)

• Production: Granulation, compression, coating, line operations.
• QC / ADL: HPLC analysis, method validation, routine QC testing.
• QA: QMS, deviation/CAPA handling, audit readiness.
• PPMC: Production planning, material coordination, inventory skills.
• IT: Support for LIMS, QMS software and infrastructure.

How to stand out

• Highlight USFDA/MHRA exposure (if any).
• For QC/ADL roles, list hands-on HPLC/GC experience and method validation exposure.
• For Production/PPMC: describe shift handling, planning tools, and SAP or ERP familiarity.
• For IT: mention experience with LIMS, CSV or GMP software implementations.

3) Lupin Ltd. — Multiple Openings (Mandideep, Bhopal, MP)

Apply / Send CV: parichaymdp@lupin.com & chetanchouhan@lupin.com
Register: https://forms.office.com/r/y3vtviV3Yf

Key departments & sample roles

• Quality Control (API): Officer / Executive — B.Pharm / M.Sc. (2–6 yrs for Officer; 8–10 yrs for Exec)
  • HPLC/GC knowledge; in-process/assay/RM/FP analysis; OOS/OOT handling; instrument qualification/csv.
• Quality Control (Micro – API): Sr. Executive — M.Sc Microbiology (11–15 yrs)
  • Stability testing, COA approvals, method validation, LIMS/QAMS exposure.
• Electrical (API): Officer — B.E. Electrical (2–6 yrs)
  • Preventive maintenance, project support, BOQ, SAP PR/PO, MIS reporting.
• Civil (FML): Officer / Executive — B.E Civil (2–6 / 8–10 yrs)
  • Facility upkeep, epoxy flooring, painting, GMP-area maintenance, SAP exposure.
• Instrumentation / Mechanical: Officers/Executives with experience handling PM, breakdowns, HVAC, CSV and CAPA.
• Mechanical (FML): Diploma / B.E roles — preventive maintenance, equipment qualification, SAP PM.

Must-haves

• 60% marks (if experience <5 years).
• No interviews at Lupin in last 6 months.
• USFDA & MHRA regulatory exposure mandatory for many roles.

Interview advice for Lupin

• Prepare documentation examples: CAPA, change control, OOS investigations, equipment qualification (DQ/IQ/OQ/PQ).
• For instrumentation, be ready to discuss PLC, SCADA troubleshooting and CSV examples.
• For microbiology, have stability and COA review examples.

4) Aurenyx PharmaTech — GMP Software Trainer

Position: GMP Software Trainer (Overseas Clients) — QA Department
Qualifications: B.Pharm / M.Pharm (Mandatory)
Experience: 0–1 year (QA) — Freshers considered
Location: Pune
Requirements: Male candidates only, passport mandatory (include passport no. in email)
Salary: ₹20,000 – ₹25,000 (based on interview & competency)
Apply / Send CV: hr@cyclonepharma.com (Note: company email suggests Cyclone Pharma HR)

About the role

Aurenyx provides paperless GMP software solutions. As a GMP Software Trainer, you’ll:

• Train overseas clients on GMP software workflows and CSV basics.
• Support QMS and CSV related training materials.
• Communicate clearly in English and handle client demos.
• Work closely with QA and implementation teams.

Who should apply

• B.Pharm / M.Pharm grads with strong English communication.
• Candidates with basic CSV and QMS understanding and computer literacy.
• Passport holders who can travel for client training.

Pro tips

• Include your passport number and readiness for immediate joining in your application email.
• Prepare a one-page training outline for a sample GMP software module to showcase during interview.

5) Rusan Pharma Ltd — Urgent Openings (Quality Control & Production for Injectables)

Location: Selaqui, Dehradun — Khasra no. 122 MI, central Hope Town, Selaqui, Dehradun – 248197
Apply / Send CV: brijendra.sengar@rusanpharma.com | paridhi.sharma@rusanpharma.com
Contact: 9105050157

Open roles

• QC – Micro: M.Sc Microbiology / B.Sc — 4–6 yrs (Officer)
• QC – HPLC: M.Sc Chemistry — 4–6 yrs (Officer / Sr. Officer)
• Production (Injection): B.Pharm — 4 yrs (Officer)
• Operator (Injection): 12th & ITI — skills in visual, washing, terminal, filling operations

What Rusan expects

• Injectable experience — terminal sterilization, aseptic techniques, filling and washing lines.
• HPLC hands-on experience for QC roles.
• Strong adherence to aseptic GMP and documentation.

6) Leben Life Sciences — Regulatory Affairs Trainee

Position: Regulatory Affairs Trainee
Qualification: M.Pharm (specialization in Regulatory Affairs preferred)
Experience: 0–1 year (freshers encouraged)
Location: Akola, Maharashtra — On-site, Full-time
Apply / Send CV: career@lebenlifesciences.com (Subject: “Regulatory Affairs Trainee Application”)
Contact for queries: 7498035480

Role highlights

• Support dossier preparation and regulatory submissions (CDSCO, EU GMP awareness).
• Monitor regulatory updates and help with labeling, documentation and audit prep.
• Liaise with authorities and assist QA for compliance tasks.

Why apply

• Strong entry-level exposure to global regulatory frameworks.
• Hands-on training and opportunity for fast career growth in regulatory affairs.

How to apply — resume & email templates that get noticed

Below are concise, recruiter-friendly templates you can copy and use immediately.

Resume checklist (bring to walk-ins):

• 3–5 page polished resume (1–2 pages preferred for freshers).
• Passport (for Aurenyx), Aadhaar, PAN, degree certificates, experience letters, relievers.
• Latest salary slip & notice period certificate.
• 2 passport photos.
• Original + 2 xerox sets of documents.

Email subject line templates (use exact role & location):

• Optimus: Application — Graduate Trainee (API Production) — Optimus Drugs Unit 3 — [Your Name]
• Stallion: CV — QC/ADL/Production — Stallion Laboratories Unit II Bavla — [Your Name]
• Lupin: Application for [Role] — Mandideep — [Your Name] — (B.Pharm/M.Sc)
• Aurenyx: GMP Software Trainer Application — Passport: [Passport No] — [Your Name]
• Rusan: Application — QC (HPLC)/Production (Injectables) — Rusan Pharma — [Your Name]
• Leben: Regulatory Affairs Trainee Application — M.Pharm — [Your Name]

Short email body (copy & paste)

Dear [Hiring Manager Name],

Please find attached my resume for the position of [Exact Role]. I have [X years] experience in [relevant skill, e.g., HPLC analysis / API production / GMP training]. I am available for immediate joining and can attend the walk-in interview on the specified dates.

Attached: Resume, Degree Certificate, Experience Letter, ID Proof.

Regards,
[Full Name] | [Mobile No] | [Email] | [Location]

Interview checklist — what to carry & be ready for

1. Printed resume (3 copies) and original certificates.
2. Experience letters and relieving letter if applicable.
3. Latest salary slip, ID proof (Aadhaar/PAN/Passport), and two passport photos.
4. Pen, notepad, and a clean folder.
5. Mask and personal safety kit if traveling.
6. Be ready for group discussion or small practical test (HPLC knowledge, basic calculations, or simple troubleshooting questions).

Role-specific interview prep & example answers

API Production — Common questions

• Q: Describe a batch you operated.
  A: Give structure: batch size, your exact tasks (charging, reaction control, critical parameters like temp/pH), any deviation and corrective action, documentation done (BMR/BPR).
• Q: How do you handle a deviation during reaction?
  A: Explain immediate containment, inform QA, document deviation, collect samples, and root-cause analysis with CAPA.

QC / HPLC — Common questions & demo

• Q: Explain HPLC system suitability parameters and acceptance criteria.
  A: Discuss plate count, tailing factor, resolution, %RSD for replicate injections.
• Q: How do you investigate an OOS?
  A: Outline lab review, sample integrity checks, method verification, repeat analysis, and escalate to QA.

QC-Microbiology

• Q: How do you perform a sterility test?
  A: Explain sampling, aseptic transfer, incubation, and how you document and interpret results.
• Q: How do you manage a contaminated stability sample?
  A: Trace root cause, check sampling chain, lab practices, and document CAPA.

Instrumentation / Electrical / Mechanical

• Q: Troubleshoot a PLC alarm — what steps?
  A: Check wiring/power, I/O diagnostics, ladder logic, and history logs; collaborate with instrument engineer and document actions.

GMP Software Trainer (Aurenyx)

• Q: What is CSV?
  A: Computer System Validation — evidence that IT systems perform intended functions as per GMP; explain basic validation lifecycle (requirements, IQ/OQ/PQ).
• Q: How would you train an overseas client with limited English?
  A: Use simple language, visual aids, role-play, and recorded demos; follow up with written SOPs.

Regulatory Affairs Trainee

• Q: What’s in a dossier for regulatory submission?
  A: Administrative info, drug master file, stability data, COA, manufacturing process, analytical methods, labeling.
• Q: How would you track regulatory changes?
  A: Use official regulator bulletins, subscribe to CDSCO/EU GMP updates, maintain an internal regulatory tracker.

Salary expectations & career trajectory (India — rough guide)

Note: Salaries vary by company size, city, experience, and role. Figures below are indicative ranges for India in 2025.

• Graduate Trainee / Jr. Production (API): ₹18,000 — ₹35,000 per month
• QC / Jr. Executive (HPLC): ₹20,000 — ₹40,000 per month
• QC-Micro / Sr. Executive: ₹40,000 — ₹80,000 per month (senior roles higher)
• Instrumentation / Electrical / Mechanical Officers: ₹30,000 — ₹70,000+ per month depending on experience
• GMP Software Trainer (Entry): ₹20,000 — ₹25,000 per month (as listed)
• Regulatory Affairs Trainee (M.Pharm): ₹20,000 — ₹35,000 per month initially

Career growth: Start as Executive/Officer → Senior Executive → Team Lead → Manager → Head of Department. Regulatory and QA paths often lead to global roles with higher pay and international exposure.

How to craft a strong CV (pharma-focused)

1. Header: Name, contact, LinkedIn (if any), location.
2. Professional Summary (2–3 lines): Focus on role + years + strongest skill (e.g., HPLC, API reaction ops, GMP compliance).
3. Key Skills: HPLC, GC, BMR/BPR, GMP, IPC, CSV, LIMS, GAMP, PLC, SCADA, SAP PM.
4. Experience: Bullet points focusing on achievements & metrics (e.g., “Reduced batch downtime by 12% by optimizing drying cycle”).
5. Education: Degree, college, year, percentage. (Note Lupin: 60% required if experience <5 yrs).
6. Certifications: GMP training, HPLC method validation course, CSV basics, safety training.
7. Projects / Internships: Briefly explain production runs, validation tasks, or software deployments.

Walk-in strategy — convert walk in to offer

• Reach early; be calm and professional.
• Dress professionally; pharma prefers business casual or lab-appropriate attire.
• Keep answers structured (Situation, Task, Action, Result).
• Offer immediate joining if possible — many roles prefer immediate joiners.
• Follow up with a polite email after the walk-in thanking them and restating interest.

Frequently Asked Questions (FAQs)

Q: Do I need original certificates for walk-ins?
A: Yes — carry original documents for verification, plus photocopies.

Q: What is immediate joining?
A: Availability to start within 7–15 days; some roles ask for 24–48 hours.

Q: Are freshers eligible?
A: Yes — Stallion, Lupin & Leben list roles for freshers and up to 0–1 year entry-level positions; Aurenyx and Leben explicitly encourage freshers for specific roles.

Q: Is regulatory exposure mandatory?
A: For Lupin senior roles & specific QC/QA roles, USFDA/MHRA exposure is mandatory.

Q: What to expect on the day?
A: Short screening, HR round, technical round; sometimes a written test or practical demonstration for QC/instrumentation.

Q: How to register for Lupin?
A: Apply by emailing parichaymdp@lupin.com & chetanchouhan@lupin.com and register on the provided Microsoft Forms link.

Final checklist before attending any of these walk-ins

• Updated resume (PDF + printed copies)
• Cover email saved as draft for instant sending after walk-in
• Originals and 2 sets of photocopies of: degree, marksheets, experience letters, ID proof, passport (if required), PAN, Aadhaar
• 2 passport-size photographs
• Pen, small notepad, and a calm, confident mindset