Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
The role
The main purpose of the role is to organise team activities and carry out routine and where necessary non-routine AS laboratory procedures in an effective and efficient manner and to ensure compliance with relevant Company, local and international Regulatory and Client requirements at all times.
Responsibilities
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The job holder has direct people management responsibilities for their team members and ensuring that all KPIs, targets and any other deadlines are met individually and by the team.
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Responsible for the leadership of team of designated personnel within the Analytical Development group ensuring delivery of method development and validation activities, written and oral communication of technical aspects of analytical analysis to internal and external customers in accordance with agreed service levels.
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To manage and process all HR and departmental documentation for the team members including; attendance sheets, overtime forms, sickness related documents, absence request forms and annual leave and staff appraisals including 1:1s, probationary reviews and PMRs.
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To professionally and consistently conduct all relevant Team Leaders’ activities, including managing and recording as required, performance, absence, timekeeping, holidays, grievance, discipline, training and development, etc.
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To ensure the training and development of the Team is fully delivered, understood and evidenced in line with both day to day and Company requirements.
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To organise team activities to perform routine laboratory procedures and to oversee laboratory work within the team.
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To authorise technical documentation and to routinely participate in batch release procedures in relation to the team’s activities. This may extend to other areas within the department, as required.
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To prepare technical documentation within the department, as required.
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To appraise staff within the team, including setting and assessing achievement of objectives.
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To train others as required, to ensure that all members of the Team are adequately trained, and to ensure that appropriate training records are maintained for the team.
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To maintain sectional expenditure within budgetary constraints.
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To maintain a thorough understanding of international regulatory and ISO requirements pertinent to the team and to ensure that all work within the team complies with these, with departmental procedures and the principles of Good Manufacturing Practice.
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To ensure that all sectional lead times, including those of sub-contract facilities providing a service to the team and team investigations, deviations and change controls are complied with, subject to there being no attenuating circumstances.
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To carry out and manage projects within the department and at international level, as required.
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To develop and validate laboratory procedures within the team and with other organisations, as required.
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To review analytical and laboratory data within the department for accuracy, completeness and compliance with documented procedures.
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To ensure that all health and safety procedures within the team are adhered to with respect to personal duties and the duties of others.
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To communicate effectively with other groups on site, and to participate with them in problem solving activities as required.
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To carry out any other tasks which may be required from time to time.
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Identify self-development needs for future performance and development needs for team members/direct reports.
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To undertake such tasks and to manage specific internal or ad hoc projects as and when required to meet department and business needs and within the scope of the job-holder’s capabilities and responsibilities.
Requirements
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GMP Skill Level 1 is essential for this role
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Degree educated in a scientific subject (preferably Chemistry or Microbiology)
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Excellent written and verbal communication skills
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Similar level supervisory experience within a laboratory environment essential, ideally in a pharmaceutical company
Benefits
At PCI, we believe that our employees are our most valuable asset. That's why we are committed to providing a benefits package designed to support your well-being and enhance your overall quality of life. Here's what we offer:
- Employer Pension: Secure your future with our employer pension scheme (above statutory pension).
- Competitive Salaries: We offer competitive salaries that reflect your dedication and contributions.
- Generous Annual Leave: Enjoy 25 days of annual leave, plus bank holidays.
- Family Friendly Benefits: Enjoy a range of benefits designed to support your family life.
- Employee Referral Scheme: Know someone perfect for our team? Refer them and receive £500 as our way of saying thank you!
- Staff Engagement: We value your dedication with recognition schemes and long-service awards.
- Health and Well-being: Your health matters. Count on our support with generous sick pay, access to a 24/7 GP through our employee assistance program, mental health support, and life assurance up to 4 times your annual salary.
- On-Site Subsidized Canteen.
- Cycle to Work Scheme.
- Development Opportunities: Invest in your future with our training programs, coaching opportunities, LinkedIn Learning, and further education options.
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Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Diversity, Equity, and Inclusion (DEI) are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
What We Do
PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.
