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Key Roles & Responsibilities:
* Supervise the manufacture defined cGMP procedures to deliver high potency ADC/API’s in support of launched products and clinical trial programme.
* Proactive approach to suite readiness, structured monitoring, line clearance, BOM /Stock levels, sample control and SAP inventory.
* Takes on a key role with the introduction of new products, liaising and communicating with relevant departments on highlighted issues.
* Ensuring all team members are adequately trained and deliver training as and when required.
* Effectively utilise and motivate manufacturing team to obtain the required schedule adherence.
* Possess good verbal and written communication skills.
* Ensure that all GMP documentation is completed “real time” and accurately in the aim of right first time.
* Maintain high SHE Standards, carrying out all work in accordance with appropriate SHE systems.
* Ensure that 5’s and housekeeping standards are adhered to, and suites are “audit” ready at all times.
* Raise any deviations and REW’s as required. Progress any investigations, CAPA’s to completion through “Trackwise” within the stated timeframe.
* Leads continuous progress within the suites.
* Deputy for Shift Team in their absence.
Key Competencies:
* Teamwork - As a team member, the ability and desire to work cooperatively with others on a team.
* Communication - The ability to ensure that information is passed on to others who should be kept informed.
* Building Collaborative Relationships - The ability to strengthen partnerships with others inside the organization who can provide information, assistance, and support.
* Attention to Detail - Ensuring that one’s own and others’ work and information are complete and accurate.
* Personnel Credibility - Demonstrated concern that one be perceived as responsible, reliable, and trustworthy.
* Forward Thinking - The ability to anticipate the implications and consequences of situations and take appropriate action to be prepared for possible contingencies.
* Interpersonal Awareness - The ability to notice, interpret, and anticipate others’ concerns and feelings, and to communicate this awareness empathetically to others.
* Customer Awareness - The ability to demonstrate concern for satisfying one’s external and/or internal customers.
Qualifications
Essential Qualification:
* Degree in a scientific subject or the equivalent GMP experience.
* Possess good verbal and written communication skills.
Essential Experience:
* Good chemical/bio-processing industry knowledge.
* Good working knowledge of GMP.
* Understand chemical unit operations and process chemical reaction hazards.
* Possess good verbal and written communication skills.
* Experience of working in clean rooms (desirable).
About Us
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal Employment Opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
About The Team
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle.
Seniority Level
Mid-Senior level
Employment Type
Full-time
Job Function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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