Media Filling Process Technician

About the Company:

Innopharma Technical Services, part of Innopharma Group, specialise in the training and provision of highly skilled, project-ready, Contract Engineers & Scientists to the (Bio) Pharmaceutical and MedTech Manufacturing Sector.
We are now seeking a Media Filling Process Technician to join our Global Multinational Client Site in Co. Dublin.

Location: Dublin
Contract Type: 6 months (possibility of extension)

About the Role:

This role is responsible for the operation, cleaning and upkeep of all equipment and facilities in an
aseptic environment in support of manufacturing requirements adhering to and leadership of all
cGMP, training and safety standards for the work area.

Key Responsibilities:

• Adhere to procedures and practices and maintain compliance with applicable departmental, corporate, industrial, health & safety and regulatory requirements.
• Strictly adhere to the gowning philosophies for all cleanroom, production and facility areas and take immediate action and report for all non-conformances.
• Take ownership for the setup, coordination, regulation and troubleshooting of processing equipment in an aseptic biologics processing environment for plasma derived pharmaceuticals.
• Accountable for the cleaning (Manual and automated CIP/SIP) and upkeeping of all associated facilities and equipment thereby ensuring all areas are maintained in proper working order.
• Responsible for the accuracy and completeness of all Company documentation and material reconciliation.
• Maintaining a safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures (SOPs); complying with legal regulations and monitoring environment.
• Ability to operate automated Scada-controlled/windows-based control systems in a GMP environment.
• Actively involve in the Company’s Continues improvement program by providing suggestions and implement improvement measures to optimize production methods, equipment performance, facility layout, and quality of product.
• Co-operate and support quality investigations and contribute to CAPA reporting and closure.
• Providing guidance and hands-on training to peers and colleagues and ensuring all training records are up to date and in line with training SOP’s, OJT’s and policies.
• Capability in maintaining production without supervision and effectively manage anticipating and adjusting for any interventions.
• Meeting planning targets and supply chain requirements while improving on work practices adjusting for multiple changing priorities.
• Making decisions specific to their area of work in a timely manner.
• Ability to utilize MRP systems and complete batch-specific transactions on time.
• Ensure assigned activities for a Start Up Project and Commercial facility are completed accurately and in a timely manner as per requirements.
• Performs other duties as assigned, in any area of company’s Worldwide Operations as required by the business.

What We’re Looking For:

• Bachelor’s degree (Level 8) preferably in Biology, Chemistry, Manufacturing or Mechanical Engineering or closely related scientific / technical discipline desired.
• If qualified under Level 8, a minimum of 2 years of related experience in a pharmaceutical, GMP, or EU regulated environment.
• Preferred with experience in Pharmaceuticals, Bio-pharmaceutical, Biologics Industry.
• Experience with Process equipment, aseptic process, cGMP, RABs is essential.
• Comprehensive knowledge and understanding of cGMP, EU regulations, and industry guidelines is highly preferred.
• Proactive, results oriented, and have strong attention to detail is required.
• Self-starter with strong work ethic and the ability to exercise good judgment with Critical thinking.
• Demonstrate ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.
• Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.
• Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.
• Demonstrated ability to inspire high performance in self and others and support team members around shared goals.
• Excellent verbal and written communication skills in the English language.
• Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint).

Other Specifications

• 6 Months Contract role (possibility of extension).
• Must be willing to work in Shifts as it is a shift-based role. Includes Shift premium apart with salary.
• Must be eligible to work without Critical Skills Visa sponsorship.
• Must be living in Ireland.

*Applicants must be eligible to work in Ireland.

Apply Now

If you’re passionate about manufacturing excellence and eager to grow in a fast-paced, regulated environment, we want to hear from you.

Apply Now