Job Description
* Execute defined procedures to manufacture high potency ADC/ API’s product in support of launched products and clinical trial programmed to GMP standards.
* Working effectively in an organized manner in order to adhere to the planned schedule.
* Contribute effectively to a team working environment but also have the ability and confidence to work on an individual basis within the production team.
* Accurately recording information required for batch records.
* Updating and reviewing plant documentation, from PI Sheets to SOP’S.
* Maintain high ESH Standards, carrying out all work in accordance with appropriate EHS systems.
* Have a working knowledge of risk management systems and procedures enabling escalation of deviation as appropriate.
* Demonstrate flexibility, self-control, and interpersonal awareness within the team environment.
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 Qualifications
* 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 Our Company
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 Affive 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.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities and individuals with needs related to their religious observance or practice.
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