Operations Excellence Technical Specialist
Posted on :
30-07-2024
Employer Active
1 Vacancy
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Job Description
About PSC Biotech
Who we are
PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased software solutions for Quality Management and Regulatory Inspections pharmaceuticals contract manufacturing professionals and metrology services to our clients.
Take your Career to a new Level
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of likeminded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diversecultural work setting.
Employee Value Proposition
Employees are the heartbeat of PSC Biotech we provide unparalleled empowering career development though Learning & Development inhouse training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client s expectations with regards to quality of all scalable and business unit deliverables staying under budget and ensuring timelines for our deliverables are being met.
A fantastic opportunity has arisen for an Operations Excellence Technical Specialist. The Technical Specialist will work on the Operations Excellence team reviews constraints in the current manufacturing process and delivering projects that directly combat these constraints.
Requirements
Bring energy knowledge innovation to carry out the following:
- Support the process by wholistically reviewing the how and why individual process steps are performed identifying areas where efficiencies can be made and leading projects to deliver these efficiencies
- Managing EHS and Quality investigations and overseeing batch record reviews.
- Provide technical support to Operation functions and changes.
- Lead crossfunctional problemsolving teams for troubleshooting and investigations within Vaccines IPT.
- Be responsible for the completion of continuous improvement projects to support manufacturing operations through the development of validation schedules master plans and validation protocols.
- Apply Lean Six Sigma and Lean methodologies.
- Represent the department on crossfunctional project teams.
- Adherence to highest standards for Compliance (Quality and Safety).
- Ensure compliance with site EHS policy cGMP and other business regulations and lead/coordinate Technical IPT input to risk assessments audits regulatory inspections and incident investigations.
- Ensure the highest Quality Compliance and Safety standards by participating and complying with our Manufacturing Division Quality Management System (QMS) requirements including ownership as relevant.
What skills you will need:
In order to excel in this role you will more than likely have:
- 5 years experience in a pharmaceutical or a highly regulated environment.
- B.Sc. Degree or other qualification in Biochemistry Microbiology Chemistry Engineering or a related field.
- Project management experiences in widescaled and/or complex project.
- Strong analytical and problemsolving skills
#LIAP1
Bring energy, knowledge, innovation to carry out the following: Support the process by wholistically reviewing the how and why individual process steps are performed, identifying areas where efficiencies can be made, and leading projects to deliver these efficiencies Managing EHS and Quality investigations and overseeing batch record reviews. Provide technical support to Operation functions and changes. Lead cross-functional problem-solving teams for troubleshooting and investigations within Vaccines IPT. Be responsible for the completion of continuous improvement projects to support manufacturing operations through the development of validation schedules, master plans and validation protocols. Apply Lean Six Sigma and Lean methodologies. Represent the department on cross-functional project teams. Adherence to highest standards for Compliance (Quality and Safety). Ensure compliance with site EHS policy, cGMP and other business regulations and lead/co-ordinate Technical IPT input to risk assessments, audits, regulatory inspections and incident investigations. Ensure the highest Quality, Compliance and Safety standards by participating and complying with our Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant. What skills you will need: In order to excel in this role, you will more than likely have: 5+ years experience in a pharmaceutical or a highly regulated environment. B.Sc. Degree or other qualification in Biochemistry, Microbiology, Chemistry, Engineering or a related field. Project management experiences in wide-scaled and/or complex project. Strong analytical and problem-solving skills #LI-AP1
Employment Type
Full Time
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