Downstream Manufacturing Engineer

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 cloud-based 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 like-minded 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 diverse-cultural work setting.
Employee Value Proposition Employees are the "heartbeat" of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house 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.  Role Description: Downstream Manufacturing Engineer working with Days Operations support team.
Requirements Role Functions: ·         Work as a key team member within the Downstream (DS) Integrated Process Team (IPT) to ensure on-time delivery of the production schedule while maintaining alignment with site safety and quality standards.
·         Provide oversight on material management, ensuring quality and delivery metrics related to material management are always maintained.
·         Own Quality Investigation from identification through root cause analysis ·         Provide oversight on day-to-day production quality metrics ensuring on-time documentation closure, line clearance and material management as per area SOPs.
·         Drive continuous improvement projects related to schedule, equipment, and delivery capability within the DS IPT.
·         Act as a link between the shift operations team and days team, ensuring standardisation and integration between all IPT teams.
·         Support audit readiness in the BDS and drive a permanent audit readiness culture within the team.
·         Direct Root Cause Analysis (RCA) sessions for both safety and quality related events, driving actions to closure with appropriate corrective/preventive measures.
·         Drive MPS standards within the area and ensure team alignment on same.
·         Lead/support area change controls, CAPAs, QSAT actions as relevant per work stream as well as completing documentation updates as required.
·         Provide ongoing coaching and support to cross functional team members, to share process and operational best practices.
·         Act as days operations member on process centred teams (PCT), working with technical operations and shift operations to identify, perform root cause analysis and develop corrective/ preventative actions for issues as they occur.
  Key Competencies & Experience: ·         A Level 7 Degree in Science, Engineering or other relevant disciplines/ relevant experience.
·         At least 3 years' experience in the pharmaceutical industry (preferably in Drug Substance) ·         Experiences across multiple site functions (including but not limited to Quality, Engineering, or Supply Chain) desirable but not required.
·         Experience in change management in a GMP environment.
·         Experience in technical writing for GMP documentation and quality investigations.
·         Self-motivated with excellent organizational skills ·         Excellent verbal and written communication skills ·         Proficient in Microsoft Office Tools (word/excel/PowerPoint) ·         Ability to work independently and as part of a team in a cross functional collaborative environment.
·         High level of attention to detail ·         Experience working with GMP Documentation Management Systems ·         Good interpersonal skills   Qualifications: ·         At minimum level 7 in a relevant Qualification.
#LI-EL1 Requirements Role Functions: · Work as a key team member within the Downstream (DS) Integrated Process Team (IPT) to ensure on-time delivery of the production schedule while maintaining alignment with site safety and quality standards.
· Provide oversight on material management, ensuring quality and delivery metrics related to material management are always maintained.
· Own Quality Investigation from identification through root cause analysis · Provide oversight on day-to-day production quality metrics ensuring on-time documentation closure, line clearance and material management as per area SOPs.
· Drive continuous improvement projects related to schedule, equipment, and delivery capability within the DS IPT.
· Act as a link between the shift operations team and days team, ensuring standardisation and integration between all IPT teams.
· Support audit readiness in the BDS and drive a permanent audit readiness culture within the team.
· Direct Root Cause Analysis (RCA) sessions for both safety and quality related events, driving actions to closure with appropriate corrective/preventive measures.
· Drive MPS standards within the area and ensure team alignment on same.
· Lead/support area change controls, CAPAs, QSAT actions as relevant per work stream as well as completing documentation updates as required.
· Provide ongoing coaching and support to cross functional team members, to share process and operational best practices.
· Act as days operations member on process centred teams (PCT), working with technical operations and shift operations to identify, perform root cause analysis and develop corrective/ preventative actions for issues as they occur.
Key Competencies & Experience: · A Level 7 Degree in Science, Engineering or other relevant disciplines/ relevant experience.
· At least 3 years' experience in the pharmaceutical industry (preferably in Drug Substance) · Experiences across multiple site functions (including but not limited to Quality, Engineering, or Supply Chain) desirable but not required.
· Experience in change management in a GMP environment.
· Experience in technical writing for GMP documentation and quality investigations.
· Self-motivated with excellent organizational skills · Excellent verbal and written communication skills · Proficient in Microsoft Office Tools (word/excel/PowerPoint) · Ability to work independently and as part of a team in a cross functional collaborative environment.
· High level of attention to detail · Experience working with GMP Documentation Management Systems · Good interpersonal skills Qualifications: · At minimum level 7 in a relevant Qualification.
#LI-EL1