Dr. Reddy's Laboratories Posted September 24, 2026

Team Member - Engineering (Process Mechanical)

Pydibimavaram, AP, India Full-time
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Dr. Reddy's Laboratories is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Purpose

To ensure reliable operation, maintenance, and performance of pharmaceutical manufacturing equipment by executing preventive, breakdown, and improvement maintenance activities, ensuring compliance with cGMP, safety, and regulatory requirements, and supporting uninterrupted production operations.

Roles & Responsibilities

1. Equipment Maintenance Management

Maintain and support manufacturing equipment, including: Granulation (RMG, FBD)

Compression (tablet presses)

Coating machines

Blenders, sifters, mills

Filling and packing equipment

Derma / Softgel / potent equipment (if applicable)

Ensure equipment availability, reliability, and performance to meet production targets.

2. Preventive & Predictive Maintenance

Plan and execute preventive maintenance schedules for all equipment.

Perform inspection, lubrication, alignment, and replacement of critical components.

Monitor equipment health and support predictive maintenance initiatives.

Ensure adherence to planned maintenance systems and TPM practices.

3. Breakdown Maintenance & Troubleshooting

Attend and resolve equipment breakdowns in a timely manner.

Diagnose mechanical failures such as: Bearing failures

Gearbox issues

Vibrations and misalignment

Mechanical wear and tear

Coordinate with cross‑functional teams to minimize downtime and production loss.

4. Installation, Qualification & Commissioning

Support installation and commissioning of new equipment.

Participate in equipment qualification (IQ, OQ, PQ) activities.

Ensure mechanical systems meet design and validation requirements.

5. cGMP, Compliance & Documentation

Follow cGMP, Good Engineering Practices (GEP), and SOPs.

Maintain accurate records of: Maintenance logs

Equipment history

Breakdown reports

Spare part usage

Support deviations, CAPA, change control, and audit requirements.

Ensure equipment is maintained in a validated and compliant state.

6. Spare Parts & Inventory Management

Identify and maintain critical spare parts inventory.

Ensure timely availability of spares to prevent delays in maintenance.

Coordinate with stores and procurement for spare part planning and procurement.

7. Cross‑Functional Coordination

Work closely with Production for equipment readiness and maintenance scheduling.

Coordinate with QA for compliance, documentation review, and validation activities.

Support Instrumentation and Electrical teams for integrated troubleshooting.

8. Safety, EHS & Good Maintenance Practices

Follow safety guidelines, PPE usage, and LOTO (Lock‑out/Tag‑out) procedures.

Ensure safe handling of tools, machinery, and maintenance activities.

Maintain 5S and housekeeping standards in maintenance areas.

Report and rectify unsafe conditions or practices.

9. Continuous Improvement & TPM

Participate in TPM (Total Productive Maintenance), Kaizen, and Lean initiatives.

Support Jishu Hozen (JH) activities and operator capability building.

Identify opportunities for equipment reliability improvement and cost reduction.

Drive improvement in MTBF (Mean Time Between Failures) and MTTR (Mean Time to Repair).

Educational Qualification

B.Tech in Mechanical Engineering

Experience

3–6 years of experience in equipment maintenance in a pharma manufacturing plant.

Experience in OSD / Injectables / Softgel / Derma equipment preferred.

Exposure to regulated environments (US‑FDA / EU‑GMP / WHO‑GMP) is an advantage.

Key Skills & Competencies

Strong knowledge of mechanical systems and pharma equipment

Preventive & breakdown maintenance expertise

Troubleshooting & root cause analysis (RCA)

Understanding of cGMP and validation requirements

Good documentation and compliance discipline

Basic understanding of TPM and Lean systems

Benefits Offered

At Dr. Reddy’s we actively help to catalyse 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. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.

For more details, please visit our career website at https://careers.drreddys.com/#!/"

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Pydibimavaram, AP, India
Employment type
Full-time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 2618 comparable Manufacturing & CMC roles across 164 biopharma companies.

2618Comparable roles tracked
2323Currently active
164Companies hiring similar roles
61Countries represented

Salary context

689 of 2618 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.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $0 – $314,750 (median $130,000)

Where these roles are based

Top locations among the 2618 comparable roles

United States1248
India162
Germany140
France95
Switzerland91
Netherlands89

+ 55 more countries

Seniority mix

1139 of 2618 peers have a known seniority level

Senior355
Manager276
Associate135
Principal95
Director93
Associate Director85
Intern/Fellow/Postdoc63
Senior Director33
Executive/VP4

Therapeutic area mix

12 of 2618 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease8
Rare Disease2
Respiratory1
Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Pfizer Healthcare India Private Limited Vizag, India Associate
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Director
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Director
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

40%
Associate - Equipment Maintenance
Pfizer Healthcare India Private Limited · Vizag, India · Associate
Function Therapeutic area Seniority Country
40%
Sr Associate Contract Development & Mfg
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior
Function Therapeutic area Seniority Country
40%
Contract Development & Mfg Mgr Person in Plant
Amgen Technology Pvt Ltd. · Hyderabad, India · Seniority not listed
Function Therapeutic area Seniority Country
40%
Senior Director, AIN Manufacturing Lead
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.