Job Scope
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts.
Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System.
Key Duties and Responsibilities
Coordinate with other associates daily in support of manual instruction development and production process development. All to support a quality process.
Work from documented procedures and maintain quality data.
Maintains the integrity and cleanliness of work areas.
Participate in applicable departmental and interdepartmental training.
Maintain current and effective training to standard operating procedures, work instructions, and applicable changes affecting the Reagent Manufacturing.
Assures adherence to safety.
Establish an effective working partnership with other Luminex departments to promote effective communication and transfer knowledge/experience to others.
Other duties as assigned.
Education, Experience, and Qualifications
Associate's Degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related fields required and
1+ Years Relevant in a Life Sciences, Chemistry, or Medical Technology related industry required
Standard Physical Demands
Standing - Occasionally
Stooping - Occasionally
Bending - Occasionally
Climbing - Occasionally
Sitting - Occasionally
Kneeling - Occasionally
Lifting of at least 40lbs - Occasionally
Travel Requirements
0% No travel is required.
What We Offer
Receive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.