Senior Process Manager

Quanta part of QCS Staffing; Dublin; On-site; EUR 70,000 - 90,000; Full time

Job summary

A global pharmaceutical client is seeking a Senior Process Manager in Dublin for an ambitious new facility. This role offers the chance to engage in cutting-edge technologies and enhance your skills, contributing to life-changing treatments. Applicants should possess significant experience in the pharmaceutical sector and excellent communication abilities.

Qualifications

• Minimum of 5 years’ experience for MSc or 7 years for BSc in life sciences.
• Experience with upstream cell culture and downstream purification.
• Working knowledge of statistical methods for data analysis.

Responsibilities

• Support design, construction, and qualification of manufacturing processes.
• Lead various manufacturing science and technology initiatives.
• Maintain quality and safety compliance, focusing on customer satisfaction.

Skills

Communication

Problem Solving

Continuous Improvement

Education

Bachelor's degree or higher in Biological Sciences/Chemical Engineering/Chemistry

Job description

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Senior Process Manager - Life Sciences - 11-months - Dublin

Do you want to be part of one of the top 10 best companies to work for in Ireland? If so, this could be your chance! One of our global pharmaceutical clients is looking for a Senior Process Manager to join their team in Dublin for their new large-scale facility.

This is a fantastic opportunity to be part of fast-paced project;with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.

This is a truly exciting project, which when complete will contribute to the manufacturing of a life changing treatment.


Responsibilities:

Support the design, construction and qualification of upstream & downstream equipment

Support establishment of the commercial process and routine manufacturing by:Supporting experimental design, execution, data analysis and interpretation. Interpreting trends observed in commercial process monitoring (e.g., proactive process analysis (PPA), continued process verification (CPV), statistical process control (SPC) multivariate analyses (MVDA), and for further technical investigations and process changes that seek to drive improvements to yield and/or robustness.Supporting deviation management.Supporting change control prioritisation and implementation.Authoring and reviewing of batch documentation, technical reports and global regulatory submissions.Supporting multidisciplinary teams for process improvement and troubleshooting with end-to-end product focus.Applying LeanSixSigma tools by:Securing continuity of an appropriate LSS/CEM level of knowledge.Facilitating problem solving & risk assessment (FMEA) projects/meetings.Making problems visible and strive for continuous improvement.Serving as a key member during internal audits and external inspections/audits

Lead and support various manufacturing science and technology organisational initiatives as needed

Maintain continuous focus on quality and safety compliance and unflinching focus on the customer

About you:

Minimum of 5 years’ (for MSc) or 7 years’ (for BSc)directly related experience in academia, pharmaceutical or biotechnology company – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practice

Self-starter and results focused

Excellent oral and written communication skills

Bachelor's degree or higher in Biological Sciences/Chemical Engineering/Chemistry

Proven track record in delivering excellence

Experience with upstream cell culture and/or downstream purification of biological molecules.

Experience with tech transfer, regulatory filling and commercial drug substance manufacturing of biologics is a plus

Working knowledge of statistical methods of DOE design and data analysis

Interested in this role? Apply today!

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