As the OSD Operations Leader Drug Product you will lead the production of high-quality pharmaceutical drug products in a dynamic and regulated environment. You will ensure your team consistently delivers on operational objectives compliance standards safety and continuous improvement initiatives. This is a highly visible and rewarding leadership role for individuals committed to quality and operational excellence.
Key Responsibilities:
- Oversee and execute all drug product manufacturing operations ensuring compliance with internal and external regulatory standards (including cGMP HPRA/FDA).
- Provide leadership direction and motivation to a team of 8-45 ensuring effective performance strong communication and development of team members.
- Plan staffing and material resources to guarantee smooth efficient and safe daily operations.
- Coordinate onboarding training and ongoing skills development for team members.
- Monitor and manage key performance indicators for the department (e.g. yield production rate resource usage attendance overtime).
- Maintain accurate records and timely updates in manufacturing and personnel systems.
- Foster a culture of safety quality innovation and continuous improvement throughout the manufacturing area.
- Collaborate with other shift leaders and cross-functional teams to deliver operational results and support site-wide projects.
- Lead and support facility and equipment/process improvements and Operational Excellence (OpEx) initiatives.
- Ensure compliance with safety environmental and quality SOPs and manage adherence to all relevant procedures policies and regulations.
- Support HR processes including performance management annual reviews and employee relations.
- Lead the department in preparation for internal and external regulatory inspections/audits.
- Demonstrate flexibility regarding shift work and working hour requirements to meet business demands.
Qualifications :
- Previous experience in pharmaceutical manufacturing (Oral Solid dose experience preferred.)
- Strong leadership communication and organizational skills.
- Proven ability to manage teams and optimize operational performance.
- Diploma in a relevant science or engineering discipline and/or significant relevant experience.
- At least 3 years of experience in batch processing within an FDA/HPRA regulated industry including thorough knowledge of cGMP and pharmaceutical regulatory standards.
- Minimum 3 years of supervisory experience in a highly automated manufacturing environment preferably with demonstrated experience leading process improvements.
- Strong communication and interpersonal skills with a commitment to quality accuracy and a Right First Time ethos.
- Proven problem-solving abilities a continuous improvement mindset and a strong work ethic with integrity.
Additional Information :
Why Join Us
- Work in a forward-thinking innovative pharmaceutical setting with opportunities to make a tangible impact
- Be part of a high-performance team culture with a focus on development and excellence
- Competitive compensation benefits and career advancement potential
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
As the OSD Operations Leader Drug Product you will lead the production of high-quality pharmaceutical drug products in a dynamic and regulated environment. You will ensure your team consistently delivers on operational objectives compliance standards safety and continuous improvement initiatives. T...
As the OSD Operations Leader Drug Product you will lead the production of high-quality pharmaceutical drug products in a dynamic and regulated environment. You will ensure your team consistently delivers on operational objectives compliance standards safety and continuous improvement initiatives. This is a highly visible and rewarding leadership role for individuals committed to quality and operational excellence.
Key Responsibilities:
- Oversee and execute all drug product manufacturing operations ensuring compliance with internal and external regulatory standards (including cGMP HPRA/FDA).
- Provide leadership direction and motivation to a team of 8-45 ensuring effective performance strong communication and development of team members.
- Plan staffing and material resources to guarantee smooth efficient and safe daily operations.
- Coordinate onboarding training and ongoing skills development for team members.
- Monitor and manage key performance indicators for the department (e.g. yield production rate resource usage attendance overtime).
- Maintain accurate records and timely updates in manufacturing and personnel systems.
- Foster a culture of safety quality innovation and continuous improvement throughout the manufacturing area.
- Collaborate with other shift leaders and cross-functional teams to deliver operational results and support site-wide projects.
- Lead and support facility and equipment/process improvements and Operational Excellence (OpEx) initiatives.
- Ensure compliance with safety environmental and quality SOPs and manage adherence to all relevant procedures policies and regulations.
- Support HR processes including performance management annual reviews and employee relations.
- Lead the department in preparation for internal and external regulatory inspections/audits.
- Demonstrate flexibility regarding shift work and working hour requirements to meet business demands.
Qualifications :
- Previous experience in pharmaceutical manufacturing (Oral Solid dose experience preferred.)
- Strong leadership communication and organizational skills.
- Proven ability to manage teams and optimize operational performance.
- Diploma in a relevant science or engineering discipline and/or significant relevant experience.
- At least 3 years of experience in batch processing within an FDA/HPRA regulated industry including thorough knowledge of cGMP and pharmaceutical regulatory standards.
- Minimum 3 years of supervisory experience in a highly automated manufacturing environment preferably with demonstrated experience leading process improvements.
- Strong communication and interpersonal skills with a commitment to quality accuracy and a Right First Time ethos.
- Proven problem-solving abilities a continuous improvement mindset and a strong work ethic with integrity.
Additional Information :
Why Join Us
- Work in a forward-thinking innovative pharmaceutical setting with opportunities to make a tangible impact
- Be part of a high-performance team culture with a focus on development and excellence
- Competitive compensation benefits and career advancement potential
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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