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Sunday, 26 May 2024 06:00

Validation Engineer/Manager

  Le Sueur, MN,  United States |  Full-time regular

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Posting Date :  2024-03-15

Job Identification :  135

Department  :  Validation

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The Validation Engineer/Manager  reports to the Director of Operations (with a dotted line reporting responsibility to the Director of Technical Operations) and is responsible for the execution and regulatory compliance of the validation program.  The Validation Manager is well-versed in the generation, execution, modification, and summation of Validation documents to ensure Good Documentation Practices within pharmaceutical operations. This role serves to ensure products and processes are maintained in a validated state and compliant with regulatory and cGMP requirements throughout the product lifecycle. This is accomplished through interaction and coordination of activities with all relevant departments within the organization.   


Role Specific Requirements:

  • Review, plan, schedule and organize validation projects for new and existing areas, including manufacturing equipment, processes, plant systems, storage facilities and equipment. 
  • Develop and implement all necessary standard operating procedures for validation of plant processes, equipment installation and operational qualification (IQ/OQ), performance qualification (PQ), requalification and revalidation of critical systems and utilities.
  • Design IQ/OQ/PQ and validation campaigns, develop, prepare, and write the protocols for process validation, equipment validation, cleaning validation, IQ/OQ and performance qualification.
  • Coordinate validation and IQ/OQ/PQ activities with production, quality control laboratories and outside contractors providing leadership, training, and guidance.
  • Review and analyze moderately complex analytical and physical data generated from validation activities.  Write validation final reports that present, summarize, and offer conclusions on the validity of the process based on the results of the analysis and obtain necessary approvals on a timely basis. 
  • Coordinate the facility qualification program by preparing the protocols, monitoring the execution, auditing the results, and assisting production in resolving any identified problems.
  • Recommends validation approaches / strategies, priorities, and resources required.   Accountable for accuracy and integrity of protocols, reports and documentation generated to meet regulatory authorities, accountable for meeting critical deadlines for complex projects.
  • Provides validation support for Technical Transfer from  Research and Development and supports the Regulatory Affairs Department for product submissions and regulatory filings.
  • Remain current on legislative, regulatory, and technical changes within the industry, and on training requirements within the facility.  Continually develops expertise and acts as a technical expert for the various validation and production activities.
  • Assign equipment asset number to new equipment.
  • Performs regular validation and performance qualification audits as necessary to ensure conformity to all regulatory requirements.  Identifies areas of validation failure or deviations from established process and product standards, providing recommendation to solve identified problems.
  • Participates in regulatory audits by government regulatory agencies and audits by customers.
  • Conducts Validation reviews as required during the change control process, deviation process and batch record review process.
  • Validate batch record calculations sheets as required.
  • Help develop and maintain drawings and diagrams for regulatory agencies and in plant use.
  • Support the North American Project Manager and other management in equipment selection and facility modifications. This includes supporting URS development and assisting in preparing capital equipment expense requests.
  • Support the North American EHS Manager and other management in environmental activities as required.
  • Perform other duties as assigned.



We are unable to support/sponsor any visa or immigration cases at this time.  


Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.


Competencies Required for the Role


CRITICAL THINKING – is the ability to be thoughtful and draw pertinent conclusions after a discussion or meeting; can eventually support the final outcomes and decisions.


EFFECTIVE COMMUNICATION - Is the ability to convey information to another effectively and efficiently, to listen – help facilitate sharing of information between people.  It is about understanding

the emotional intention behind the information. The ability to express oneself clearly in conversations, confirm understanding, communicate using data and facts whilst adapting to one’s audience.  Exhibit willingness to listen and show respect for oneself and others in interactions with others.   Express oneself clearly in verbal and business writing


THOROUGHNESS/DETAIL ORIENTED – Ensuring that one’s own and others’ work and information are complete and accurate; carefully preparing for meetings and presentations following up with others to ensure that agreements and commitments have been fulfilled.


PLANNING – is the process of thinking about and organizing the activities required to achieve a desired goal.


Other Requirements Essential:

Essential:

  • 7 years relevant experience in a regulated pharmaceutical industry with 5 years in a validation role
  • Bachelors degree in Science or engineering
  • Knowledge of validation strategies and execution techniques, validation requirements and regulatory expectations for GMP compliance.
  • Must possess strong customer focus and quality mind set.
  • Is a champion of compliance while balancing business results
  • Strong command of the English language; written and orally
  • Ability to work both independently and in a team.

Desired: 

  • Master’s degree in science or related field



About Bimeda:

 

Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world’s animals.


Bimeda’s global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.


Bimeda’s eleven manufacturing facilities across eight countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.


Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.


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Bimeda is a leading global manufacturer,  marketer and distributor of animal health products and veterinary pharmaceuticals.  Through ongoing expansion and strategic acquisition,  Bimeda has established markets in more than eighty countries worldwide and has R&D,  manufacturing and distribution capabilities across Europe,  North America,  South America,  Africa,  Asia and Australasia.


global

OPERATES
IN OVER
80
countries

people

950+
EMPLOYEES

lab

8
R&D
and 7
REGULATORY LABS

factory

10
MANUFACTURING
facilities in
7 COUNTRIES

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