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Manufacturing Operator I & II

Reuben Cooley Inc

Fall River, MA

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biotech and Pharmaceutical, Calibration, Change Control, Computer Systems, Control Systems, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Documentation, Drug Manufacturing, English Language, Equipment Maintenance/Repair, High School Diploma, Inventory Management, Machine Tool, Machining Operations, Maintain Compliance, Manufacturing, Manufacturing Management, Manufacturing Operations, Manufacturing/Industrial Processes, Mathematics, Metered Dose Inhalers, Operational Support, Order Picking/Packing, Organizational Skills, Performance Analysis, Preventative Maintenance, Product Packaging, Production Control, Production Machining, Production Schedule, Quality Management, Quality Metrics, Regulatory Compliance, Regulatory Requirements, Safety Process, Safety/Work Safety, Sanitation, Standard Operating Procedures (SOP), System Operations, Time Management, Warehousing
LOCATION
Fall River, MA
POSTED
23 days ago
Job Title: Manufacturing Operator 1 Work Location: Fall River, MA Reports To: Manufacturing Supervisor Purpose: The purpose of this role is to be part of manufacturing metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Scope: The scope (content and statements) of this job description is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. Multifunctional Role This job is a multifunctional role. The primary nature of this job is to serve as a Manufacturing Operator. As a secondary requirement, this position will be expected to provide support to other operational functions to include but not limited to Warehouse Operations, Packaging Operations, and Facilities Operations. Job Description: The Manufacturing Operator performs all functions relating to the production of MDI (Meted doses inhaler) products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). Incumbents in this position are responsible for the safe and efficient execution of their job duties, while ensuring product compliance to established standards. Essential Duties and Responsibilities Dispensing raw material and primary packing materials as per work order and checking of raw material and primary packing materials. Ensure the proper planning and execution of batches. Performing cleaning and sanitation of production area and machinery as per respective procedures. Daily monitoring of production performance. Perform manufacturing processes and document activities in batch records and logbooks. Machine operation with minimum rejections and maximum outputs while maintaining quality standards within the standard norms. Operating equipment and performing necessary maintenance on machinery. Ensure equipment upkeep in co-ordination with engineering for preventive maintenance and calibration. Maintaining inventory of machine parts, tools and accessories. Working individually and in collaboration with others as part of a team. Collaborate with packaging, maintenance, quality teams for cross functional activities. Ensure status labelling at all stages of manufacturing, filling and cleaning. Identifying and assisting in any corrective actions. Perform, check and ensure calibration/verification of instruments, equipment and weighing balances as per schedule. Perform line clearance checks. Wearing appropriate PPE as stated in the SOP before entering any processing areas. Following procedures to complete tasks in a safe and efficient manner. Performing duties through the proper safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Performing other related duties assigned. Be able to operate computer systems with ease. Knowledge of pharmaceutical manufacturing and related documents. Basic understanding of deviation, CAPA, change control, FMECA , OOS,OOT and OOAC. Other Responsibilities Maintaining and followed 100% cGMP, GDP and SOP Compliance during complete operation hours. Complying with all company policies and procedures. Reporting all issues that arises to the department head or reporting manager. Performing daily maintenance on equipment and machinery. Completing all documentation in a timely manner, ensuring their integrity, accuracy and completeness. Maintaining discipline in department. May be required to assist in the training of other employees in the department. Flexible to work extended hours, to achieve manufacturing schedule when needed. Training and Safety: All employees must undergo various training activities at the start of their employment. New trainings and re-trainings will occur periodically. Operators may be required cross-train in all areas of the manufacturing operations. Employees must strictly adhere to all safety, health, and environmental guidelines at all times and ensure that all safety precaution are being taken during handling of machines. Qualifications High school diploma or equivalent is required. Accredited college certificate or university degree is preferred. Minimum one (1) year of manufacturing experience in pharmaceutical industry. MDI experience is highly preferred. Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic understanding of mechanical machinery and the operating principles of control systems. Ability to follow both verbal and written instructions. Demonstrated ability to work in both independent and team environments. Good knowledge of Health & Safety procedures, including, OSHA. Strong mathematical and organizational skills. Physical Requirements This position requires the ability to do heavy lifting / bending frequently. Exert an amount of force continuously and/or up to 5 pounds of force frequently and/or up to 25 pounds of force occasionally and/or up to 50 pounds of force rarely by utilizing a hand truck to lift, carry, push, pull or otherwise move objects. Ability to wear appropriate PPE is required. Individual may be required to wear respiratory devices that include but are not limited to: Air Purifying Respirators (APR) which include half-face and full-face negative pressure respirators, hooded powered air purifying respirators, or Supplied Air Respirators (SAR), which include hooded or full face supplied air respirators.

About the Company

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Reuben Cooley Inc