Process Engineer
Process Engineer
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Job Description
Job Summary
We are looking for a Team Member Process Engineering in MSAT for coordinating preventive maintenance schedules overseeing external contractors and ensuring compliance with safety and quality standards. They review production operations train team members manage spare parts inventory and lead troubleshooting efforts to minimize downtime. Additionally they maintain budgets support technical activities and ensure regulatory compliance contributing to the efficient and reliable operation of equipment and facilities.
Roles & Responsibilities
You will be responsible for overseeing all operations in accordance with established SOPs protocols and any cGMP documents ensuring data is captured in relevant documents following Good Documentation Practices.
You will be responsible for performing risk analysis before implementing any changes in the production area to mitigate potential hazards or disruptions.
You will be responsible for ensuring assimilation qualification and validation of new processes or technologies in production documenting and sharing findings with relevant team members.
You will be responsible for improving yields solvent recovery waste reduction and other production objectives to enhance operational efficiency.
You will be responsible for initiating and closing change control action plans to manage modifications effectively within the production environment.
You will be responsible for enhancing quality in both process and finished goods through continuous improvement initiatives.
You will be responsible for investigating incidents outofspecification (OOS) outoftrend (OOT) occurrences and complaints to identify root causes and implement corrective actions.
You will be responsible for troubleshooting issues to ensure process robustness aiming to find permanent solutions for operational challenges.
You will be responsible for ensuring that all site objectives for Safety Health and Environment (SHE) are met maintaining a safe working environment.
You will be responsible for reviewing batch production records batch cleaning records electronic batch production records (eBPRs) and electronic batch control records (eBCRs) for compliance and accuracy.
You will be responsible for preparing and reviewing Process Performance Qualification (PPQ) protocols/reports Continued Process Verification (CPV) protocols/reports and Batch Production Records (BPRs) for existing products undergoing changes.
You will be responsible for ensuring that trial recommendations are accurately captured in the validation batch production record for operational convenience and compliance.
You will be responsible for adhering to established cGMP and safety protocols during all operations reporting any deviations or incidents promptly.
You will be responsible for reporting nearmiss accidents to the appropriate Production Superior for investigation and corrective action.
You will be responsible for documenting and reporting process/system deviations to Quality Assurance (QA) participating in investigations and implementing corrective actions as necessary.
You will be responsible for executing and monitoring the commercialization of Critical Process Parameters (CPP) processes to ensure consistency and quality in production.
You will be responsible for attending mandatory training classes on cGMP SOPs process and operational safety to maintain compliance and competency.
You will be responsible for verifying temperature tuning completion before starting up trials or validation batches to ensure process integrity and accuracy.
Qualifications :
Educational qualification: Bachelors in Engineering or a related field
Minimum work experience: 57 years of experience in the pharmaceutical industry with a focus on manufacturing and engineering.
Skills & attributes:
Technical Skills
Proficiency in supporting manufacturing and delivery processes incident investigation and CAPA (Corrective & Preventive Action) implementation.
Strong understanding of process safety principles and risk assessment methodologies.
Experience in driving continuous improvement initiatives to enhance quality capacity and productivity.
Behavioural skills
Attention to detail and strong organizational skills.
Ability to work collaboratively in a crossfunctional team environment.
Excellent communication and interpersonal skills.
Additional Information :
About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddys Laboratories we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence we are a leading force in the pharmaceutical industry.
We operate 19 stateoftheart manufacturing plants across Hyderabad Vizag Baddi Mexico Shreveport and Mirfield comprising 8 OSD facilities 3 Injectables facilities and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1150 drug master files across key therapy areas such as Oncology Cardiovascular Central Nervous System and AntiDiabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally Hyderabad as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.
Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys 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. Reddys why they come to work every day and theyll say because Good Health Cant 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 were 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 Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
