Overview
Dunbar Pharmaceuticals is a newly licensed, Irish-owned pharmaceutical manufacturing company in Athlone that produces high-quality, niche ingredients for the pharmaceutical industry. We operate a new, state-of-the-art manufacturing facility with high-spec equipment and are committed to providing our customers with exceptional service and products.
Closing Date
Closing Date: July 15
The Role
We are seeking a highly motivated and experienced GMP production professional (Process Scientist) to join our operations team at our newly licensed GMP site, servicing a niche, fast-growing global industry with APIs. Working with a collaborative and dynamic team of innovators and experienced pharmaceutical industry leaders, you will be responsible for ensuring the uninterrupted supply of commercial products, directly manufacturing products within our GMP facility.
We welcome applicants with 5+ years of GMP experience to apply. We especially welcome those who are interested in organic chemistry, ambitious, hard-working and willing to learn and accelerate their career.
Key responsibilities
Perform manufacturing activities in Grade D GMP areas as required.
Operate and monitor advanced equipment used in the manufacturing process.
Perform various manufacturing activities in compliance with GMP and SOPs, including weighing, charging, reconcillation, and sampling of raw materials and finished products.
Maintain accurate and up-to-date manufacturing documentation, including batch records, logbooks, and SOPs.
Conduct routine checks and inspections of equipment and production areas, and identify and report any deviations or issues to the production supervisor.
Participate in training activities and maintain knowledge of GMP and SOPs, and proactively identify opportunities for continuous improvement.
Review and receipt incoming materials and inventory, verifying all documentation (e.g., certificates of origin, technical specifications) to ensure compliance with company policies.
Coordinate material storage, staging, and retrieval for production processes, monitoring storage integrity.
Manage inventory levels to support continuous production, ensuring appropriate stock levels and tracking expiration dates for raw materials.
Work collaboratively with the production team under the guidance of the quality team to meet production targets and deadlines, and ensure high-quality products are manufactured in a timely and efficient manner.
Adhere to safety procedures and ensure that work is performed in a safe and responsible manner.
Perform other duties as assigned.
Ensure that all documentation related to each task above is performed as per the operating procedure.
Operate components and equipment as per instructions.
Carry out cleaning activities.
Carry out material transfer activities and material intake procedures.
Keep accurate, legible records and support document creation.
Adhere to company policies and practices as laid down and trained and maintain a high standard of cleanliness whilst carrying out procedures.
Flexible in approach to work.
Minimum qualifications
3+ years experience in GMP Environments.
GMP knowledge and API manufacturing experience.
Ambitious and willing to learn new techniques and technologies.
Excellent communication skills, both written and verbal.
Ability to work effectively in a team environment.
Strong problem-solving skills.
Detail-oriented and able to work with a high degree of accuracy.
Ability to prioritise and manage multiple tasks effectively.
Reporting Structure
The Process Scientist will report to the Director of Operations.
What We Offer
We offer a competitive salary and benefits package, as well as opportunities for rapid career advancement. As a new and innovative start-up, you will work with dynamic and experienced leaders in the industry, gaining ample experience and exposure to cutting-edge technologies and techniques. You will have the opportunity to work in a fast-paced environment and collaborate with a small, collaborative and dynamic team of innovators.
Additional Information
To be considered for this position in Ireland you need to be legally eligible to work in Ireland.
To be considered for this position you need to be fluent in English.
Equal Opportunity Employers
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Dunbar Pharma is committed to celebrating this, in all its forms. We strive to build a culture that encourages, supports and empowers our employees.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
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