Dr. Reddy’s Laboratories: Project Manager — Hyderabad, TS, India
Dr. Reddy’s Laboratories lists a Project Manager opening in Hyderabad, TS, India. The position is listed as full-time. The job description covers quality control, quality assurance, manufacturing, regulatory affairs, risk management, project management, stakeholder management.
Recruitment overview
| Organisation | Dr. Reddy’s Laboratories |
|---|---|
| Post / role | Project Manager |
| Employment type | Full-time |
| Notification / job ID | REF28040Z |
| Job location | Hyderabad, TS, India |
| Work arrangement | On-site |
| Educational qualification | Degree / qualification: Educational qualification: Masters in Pharmacy/ MBA |
| Experience required | 5 years of experience preferably in Project Management Organisation or formulation development for different markets |
| Salary / stipend | See employer notice for pay details |
| Last date to apply | See official notice |
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.
The position and its setting
Dr. Reddy’s Laboratories lists Project Manager in Hyderabad, TS, India, under reference REF28040Z. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.
- Employment type: Full-time
- Employer listing date: 21 October 2026
- Job Family: Project/ Program Management
- Brands: Dr Reddy's Laboratories Limited
Responsibilities and work described
- Job Summary
- Responsibilities also include creating and maintaining detailed project information, ensuring effective coordination between cross-functional teams (CFTs), facilitating smooth workflow, and ensuring seamless communication
- Regular and accurate status reporting is essential, along with serving as the single point of contact (SPOC) for external partners and vendors for third-party assignments
- Be responsible to collaborate with stakeholders to draw up a comprehensive project plan and establish clear timelines for each milestone
- Organize project kick-off meetings and ensure adherence to the Design and Start of Development (DSN) phase gate protocols in coordination with the Quality Assurance (QA) team
- Be responsible to develop the Project Development Charter (PDC) in collaboration with the Portfolio team, incorporating the project's overall budget allocation for each year
- Be responsible for project planning & scheduling for timeline tracking and alignment with stakeholders
- Interaction with cross functional team for task monitoring, ensuring the licenses availability for all markets, availability of raw material for development, assisting the team for readiness for pilot studies and go -to-plant readiness
- Be responsible for identifying issues for de-bottlenecking
- Coordination for Pre-clinical and clinical/regulatory strategy finalisation for differing markets to ensure timely product development for scale-up and registration/Exhibit batches leading to filing and launch
- Be responsible to ensure timely project updates via MIS reports and regular presentations to senior management, facilitating task completion for timely milestone achievement
- Implementation: project schedule optimization and risk management strategies, while effectively managing budgets and prioritizing activities for seamless project progression
- Be responsible for project monitoring and control by ensuring effective risk identification and debottlenecking, prioritize activities as needed, and promptly address and resolve issues by engaging the relevant teams, including budget enhancement and execution area allocation
- Be responsible to monitor costs against deliverables, resolve conflicts, manage changes during the project lifecycle, and make key decisions based on evolving business scenarios
- Be responsible to facilitate urgency for priority project delivery, oversee coordination with external manufacturing partners, and provide support to Regulatory Affairs (RA) for document tracking and filing
- Additionally, ensure timely closure of Quality Assurance (QA) and Quality Control (QC) issues, dossier filing
Essential requirements and candidate background
- Educational qualification: Masters in Pharmacy/ MBA
- Minimum work
- 5 years of experience preferably in Project Management Organisation or formulation development for different markets
- Skills & attributes:
- Broad understanding of pharmaceutical requirements for different geographies (US, China, Russia, India, Brazil)
- Certification in Project Management/Training in Project Management
- Experience: MS projects/any other project planning software
- Behavioural Skills
- Communication and interpersonal skills
- Analytical and problem-solving abilities
- Work collaboratively with own team and cross-functional teams
Location, schedule and contract conditions
- Work arrangement: On-site
- Advertised location: Hyderabad, TS, India
Benefits mentioned by the employer
- 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
Conditions requiring the complete notice
Some passages contain complex or combined conditions that have not been reduced to short eligibility statements here. Read the complete linked notice for those passages, including any alternatives, exceptions or restrictions. The concise facts above should not be treated as the full wording of every condition.
Pay and application dates
A verified salary figure is not established in this article. An online estimate for another Project Manager vacancy is not an offer for reference REF28040Z; use the employer’s own pay disclosure and recruitment communication.
A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.
How to apply to Dr. Reddy’s Laboratories
Applications follow the official employer page linked below.
Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF28040Z.
Compare your qualifications and experience with the essential conditions for the Hyderabad, TS, India position, then read the preferred criteria separately.
Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.
Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.
Practical preparation: quality control
Quality-control experience is clearer when it describes what was checked, the acceptance basis and how a non-conforming result was handled. Include the records or review process where those were part of your work.
Relevant skills
- quality control
- quality assurance
- manufacturing
- regulatory affairs
- risk management
- project management
- stakeholder management
- communication
- pharmacy
- training
Important links
| Official notification / job description | Open official page |
|---|---|
| Online application portal | Open official page |
Read the complete official notice before applying. Availability and requirements can change.
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