Head of Operations

Posted 2 Days Ago
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Großbeeren, Brandenburg
Pharmaceutical
The Role
The Head of Clinical Operations at PCI is responsible for managing logistics, warehousing, clinical supply packaging, and labelling activities at the Großbeeren facility. This role involves ensuring compliance with GMP, SOPs, client-specific requirements, and government regulations, as well as overseeing staff training and development to enhance operational efficiency.
Summary Generated by Built In

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.

JOB OBJECTIVE:

  • The Head of Clinical Operations is responsible for the management and coordination of all logistics, warehousing, clinical supply packaging and labelling activities within the PCI Großbeeren facility, ensuring compliance with Good Manufacturing Practices (GMP), standard operating procedures (SOPs), client-specific requirements, and applicable government regulations.
  • In addition, the Head of Clinical Operations is responsible for training and development of staff to create a motivated, versatile, and trained Operations team, enabling process efficiencies, deputy roles and requirements.

TASKS:

  • Manages & supervises the Clinical Operations department responsible for (a) executing shipping requests in a timely and accurate manner (b) returns/destruction process (c) supporting the needs of clinical packaging facility.
  • Good understanding and work in compliance with AMG.
  • Ensures and verifies that finished product batches are produced in accordance with client requirements and with Good Manufacturing Practices.
  • Leads the development and implementation of systems and procedures to ensure high quality and efficient packaging and labelling operations of clinical supplies.
  • Registered with the local regulatory authority as the Head of Production of PCI Berlin Clinical Operations
  • Ensures retention of reserve samples of finished medicinal products, clinical investigational medicinal products and starting materials in accordance with §18 AMWHV.
  • Works closely with the Project Management team to provide input into the planning and execution of packaging timelines. Cross functional approach to achieve internal and external customer expectations with all departments.
  • Represents the logistics management and packaging department during all regulatory and safety audits, as required.
  • Attends client and internal project meetings as required.
  • Captures and reports on packaging operations metrics and logistics department KPIs.
  • Recommends and implements changes where necessary to improve efficiencies, reduce costs while maintaining or improving clients’ experience.
  • Develops, trains and mentors direct reports to maximize their performance and professional advancement.
  • Manages the preparation and organization of all packaging documentation in a timely manner, ensuring that it is of the highest quality and compliant with GMPs, SOPs and client-specific requirements, to ensure a smooth and accurate packaging operation.
  • Ensures and verifies that all deviations and any planned change in production and quality control have been reviewed and approved by the responsible people. Ensures that client is informed of deviations and changes and that client approval is obtained if necessary.
  • Responsible for continuous optimisation of processes.
  • Ensures required production and quality control documentation is complete and signed off by responsible personnel. Communicates packaging project status to management and co-workers, identifying problems in a timely manner with suggested solutions.
  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures and rules.
  • Manages direct reports including Warehouse Manager, Clinical Planning Manager
  • Where required, undertakes tasks and projects outside the job holder’s area of responsibility, such as expansion or new processes or equipment.

REQUIREMENTS:

  • Business or science degree or equivalent qualification.
  • Several years of experience in a similar role with demonstrable experience
  • Knowledge of GMP and GDP regulations.
  • Experience in operating ERP systems, ideally JDE (Oracle) 
  • Excellent interpersonal skills
  • Excellent team player with leadership skills
  • Business fluency in English and German
  • High flexibility or the ability to adapt, react quickly and deal with change in a fast-paced environment
  • Technical aptitude
  • Analytical approach with attention to detail

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.

The Company
HQ: Philadelphia, PA
2,259 Employees
On-site Workplace

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.

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