TSA Scientist at Phibro Animal Health Corporation
Sligo, County Sligo, Ireland -
Full Time


Start Date

Immediate

Expiry Date

11 Oct, 25

Salary

0.0

Posted On

11 Jul, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Biotechnology, Vaccines, Pharmaceuticals, Cleaning Validation, Chemistry, Product Support, Stewardship, English, Biopharmaceuticals

Industry

Pharmaceuticals

Description

ABOUT PHIBRO ANIMAL HEALTH CORPORATION

Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.
Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide.
At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.
If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.
The TSA Scientist is an integral part of our Quality team based out of our Ireland - Sligo site.

EDUCATION

 A minimum of a Masters degree in a technical discipline (e.g. biochemistry, chemistry, biotechnology, biopharmaceuticals). A PhD. is desirable.

EXPERIENCE

 At least 5 years experience in the biotechnology and/or pharmaceutical industry, with Operational experience of new product introductions and product support.
 Knowledge of the processes and equipment necessary for the manufacture of pharmaceuticals (oral solid dose), parenterals and/or biologicals
 Experience in authoring, review and execution of process validation studies and reports is a must.
 Experience with vaccines would be preferable particularly in the area of product development and stewardship.
 Experience in cleaning validation is desirable.
 Proficient in written and spoken English.

Responsibilities

 Plan and coordinate the assigned Technical Transfer (TT) activities to ensure a successful transfer of processes and technology. This will include:

  • Developing instructions relating to production operations (tableting/packaging)
  • Review and report on data relating to TT activities
  • Working with the scheduling team to schedule TT activities
  • Support the Manufacturing team throughout the manufacturing process
  • Developing protocols as required

 Focus on assigned Technical Transfer (TT) activities for new products and filling and inspection processes being transferred into the Sligo site.
 Use a risk-based approach to TT activities for planning, readiness & execution.
 Develop functional partnerships with the required site business units to address TT activity related issues.

 Continuously support the manufacturing processes through:

  • Provide on the floor process support with enhanced support during Engineering runs
  • Introduce/Establish statistically based tracking metrics
  • Continuously monitor process CPP’s and update the process databases
  • Raise, investigate and close out non conformances, planned deviations and change control requests
  • Where required performs sample analysis in accordance with standard operating procedures (SOPs)
  • Coordinates the use of external test laboratories when required
  • Present issues relating to TT and routine process monitoring activities to cross functional teams and help develop and deliver business cases for courses of action as appropriate

 Develop and maintain the depth of knowledge and commitment to excellence necessary for the manufacture of biological products.
 Conduct work activities in compliance with Safety, Health and Welfare at Work legislation and Company policies.
 Engage with and Support Quality and Regulatory Audits
Other duties as assigned

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