About the company

Memel Biotech AB is early stage supportive ATMP contract development and manufacturing organization providing end-to-end services in every
phase of the product development from pre-clinical to manufacturing through to commercialization. The team of skilled, tenacious professionals
is expanding and looking for a Senior Manufacturing Specialist to join the Manufacturing department.

About the role

As a Senior Manufacturing Specialist, you will be leading the development of the manufacturing organization and be responsible for creating procedures and processes for our manufacturing site. The role is a full-time position in Klaipeda and would be reporting directly to the Head of Manufacturing. You will be working across multiple functions daily, giving you the unique opportunity to be a part of a growing company, collaborating with highly qualified coworkers. The ideal candidate is motivated and ambitious, sharing our mission to bridge the gap between advanced therapy research and patient treatment.

Responsibilities (amongst others)

• Lead manufacturing related projects, supporting client interactions and serving as a subject matter expert.
• Manage the manufacturing facility to increase productivity. 
• Develop and optimize manufacturing procedures and processes (e.g., MBR, SOP, and work instructions) in compliance with regulatory requirements and standards.
• Supervise and train team members in cleanroom procedures.  
• Collaborate with cross-functional teams to develop and implement manufacturing strategies aligned with project timelines and goals.
• Prepare, review, and revise GMP documentation.
• Participate in risk assessments and implement risk mitigation strategies.
• Troubleshoot technical issues and implement corrective actions to maintain product quality and manufacturing efficiency.
• Comply with the company policies and quality management system.

Skills and Qualifications:

• Bachelor’s degree in a relevant area such as pharmaceuticals, biotechnology or life sciences or equivalent degree from an accredited university/ college.
• Minimum 3-5 years of experience in pharmaceutical manufacturing, preferably in ATMPs or biopharmaceutic production.
• Extensive Knowledge in application of GMP and regulatory requirements. 
• Ability to multi-task, strong analytical and organizational skills, detail oriented.
• Ability to communicate clearly and effectively with all levels of the organization and regulatory authorities.
• Strong written and communication skills in Lithuanian (mandatory) and English (mandatory).

Personal attributes

You are meticulous and detail oriented. You strive to share knowledge and support teamwork and are not afraid to take lead. You approach high-pressure situations methodically, with ease and composure. Your positive and proactive nature will be of highest importance for this position. 

Equal Opportunity Work

At Memel Biotech, we are committed to fostering a diverse and inclusive workplace where all employees, regardless notably of gender, race, religion, and age, have equal opportunities for personal and professional growth. Equality is not only a matter of social justice but also a vital component of a thriving and innovative organization. We strive to foster professional yet personable collaboration.

We offer:

• Professional career development/growth opportunities.
• Flexible working hours.
• Options for remote work when there is a need. 
• Professional development opportunities (training programs, conferences etc.).
• Full-time position with valuable work experience and excellent working conditions.
• Regular team building activities.
• Relocation package.
• Gross salary starting from 3500 Eur./month (depends on experience and competences).

Please send us your CV to info@memelbiotech.com.