Team Lead - Purification
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We're looking for an experienced and detail-oriented Team Lead - Purification to join our organization in Hyderabad, India. In this role, you will lead a team of purification specialists, overseeing the execution of purification processes while maintaining the highest standards of quality, safety, and regulatory compliance. You will be responsible for optimizing purification operations, driving continuous improvement initiatives, and ensuring that all team members are equipped with the skills and knowledge to excel in their roles.
Lead, mentor, and develop a team of purification technicians and specialists, fostering a culture of excellence and accountability
Oversee the planning, execution, and monitoring of purification processes to ensure consistent quality and efficiency
Analyze process data and performance metrics to identify bottlenecks and implement corrective and preventive actions
Ensure strict adherence to standard operating procedures (SOPs), quality standards, and regulatory requirements (GMP/cGMP)
Manage equipment maintenance schedules and troubleshoot technical issues to minimize downtime
Conduct regular performance reviews and provide constructive feedback to team members
Collaborate with cross-functional teams including quality assurance, production, and research and development
Prepare and maintain comprehensive technical documentation, batch records, and compliance reports
Drive process optimization initiatives to improve yield, reduce costs, and enhance operational efficiency
Conduct training sessions and onboarding programs for new team members
Ensure workplace safety protocols are followed and maintain a safe working environment
Report on key performance indicators and progress against operational targets to senior management
Minimum 5+ years of experience in purification operations or related field within pharmaceutical, chemical, or biotech industries
Proven experience in a team leadership or supervisory role managing technical staff
Strong expertise in purification techniques such as chromatography, filtration, distillation, or crystallization
In-depth knowledge of GMP/cGMP compliance and regulatory requirements
Proficiency in analyzing and interpreting process data using statistical tools and software
Excellent problem-solving and analytical skills with the ability to troubleshoot complex technical issues
Strong project management capabilities with experience in process optimization initiatives
Proficiency in creating and maintaining technical documentation and standard operating procedures
Knowledge of quality assurance principles and batch record management
Excellent communication and interpersonal skills with the ability to motivate and develop team members
Proficiency in relevant laboratory information management systems (LIMS) or manufacturing execution systems (MES)
Preferred: Six Sigma, Lean Manufacturing, or continuous improvement certifications
Preferred: Experience with equipment validation and qualification protocols
Preferred: Background in training and development of technical staff
About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.
With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.
With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.
Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure
Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.
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
How this role compares
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We currently track 2469 comparable Manufacturing & CMC roles across 164 biopharma companies.
Salary context
654 of 2469 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.
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Seniority mix
1064 of 2469 peers have a known seniority level
Therapeutic area mix
7 of 2469 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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