CMC Manager

Elektro; Szeligi; On-site; PLN 145,000 - 219,000; Full time

Job summary

A prominent pharmaceutical company in Poland seeks a Senior Specialist to support radiopharmaceutical development projects. The ideal candidate will have a university degree in pharmaceutical sciences, at least 2 years of experience in quality control, and knowledge of GMP requirements. Responsibilities include performing quality control testing, maintaining documentation, and collaborating effectively across departments. This role offers full-time employment with benefits including private medical care.

Benefits

Sharing the costs of sports activities

Private medical care

Sharing the costs of professional training & courses

Qualifications

• At least 2 years of experience in quality control within the pharmaceutical industry.
• Knowledge of GMP requirements.
• Experience in technology transfers and analytical method validation.

Responsibilities

• Support current and new radiopharmaceutical development projects.
• Assist in implementing and maintaining production processes.
• Perform quality control testing (HPLC, GC, TLC).
• Prepare, write, and update GMP documentation.
• Track and report project progress.
• Collaborate closely with other departments.

Skills

Quality control testing (HPLC, GC, TLC)

Problem-solving

Creative mindset

Team player

Interpersonal and communication skills

Fluency in English

Education

University degree in pharmaceutical sciences, chemistry, or related

Job description

contract of employment

full-time

senior specialist (Senior)

full office work

Additional information

Required languages:

Your responsibilities

• Support current and new radiopharmaceutical development projects at the CMO.
• Assist in implementing and maintaining production processes and quality control testing.
• Perform quality control testing (HPLC, GC, TLC).
• Prepare, write, and update GMP documentation.
• Track and report the progress of projects.
• Participate in regular internal project meetings to discuss and plan activities.
• Participate in regular meetings with contract organizations to provide project updates via teleconference or on‑site visits, as appropriate.
• Maintain records documenting all relevant communications related to projects.
• Monitor project timelines and contracts for accuracy and follow up on any discrepancies with stakeholders.
• Collaborate closely with other departments within the organization to ensure alignment and effective communication across all project areas.

Our requirements

• University degree in pharmaceutical sciences, chemistry, or a related scientific discipline.
• Knowledge of GMP requirements.
• At least 2 years of experience in quality control (HPLC, GC, TLC) within the pharmaceutical industry.
• Experience in technology transfers and analytical method validation.
• Experience in radiopharmacy will be an advantage.
• Ability to identify and solve critical problems.
• Creative mindset with the ability to think outside the box and challenge current CMC development strategies.
• Strong team player with excellent interpersonal and communication skills.
• Ability to communicate clearly and respectfully at all levels, consistently advocate for your objectives, and drive topics forward with commitment and determination.
• Willingness to travel and work within a remote, international team environment.
• Fluency in English.

Benefits

• Sharing the costs of sports activities.
• Private medical care.
• Sharing the costs of professional training & courses.