Manufacturing Operator III - Fluid Bed Dryer

Strides Pharma Inc•Chestnut Ridge, NY

5d•Onsite

About The Position

The Manufacturing Operator III performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). This is a Lead role, is considered a process expert, and is a Certified Trainer of other Operators. This role supervises the day-to-day activities of the Operators and provides guidance on tasks that are being performed on the line. Often, this position is involved in the Operator interview process but are not decision makers in terms of hiring decisions, promotions, annual evaluations, etc. Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity, and timing. Applies skills and knowledge to recognize process issues and to increase efficiency, throughput, and quality. Proactively identifies and resolves complex problems where considerable judgment is required in choosing among multiple options. Troubleshoots process issues, analyzes root causes, and makes recommendations. Understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, participates in the debrief to understand the reasons why and what needs to be corrected moving forward. Troubleshoots process issues and, as a team member, analyzes root causes and makes recommendations. Responsible for the safe and efficient execution of job duties. May serve as back-up to the Senior Manufacturing Technician.

Requirements

HS diploma with 5 years’ Pharmaceutical Manufacturing Operator experience & certification in assigned area, as required.
Forklift certification is required for certain jobs.
Knowledge of cGMPs.
Basic math, writing skills, and problem-solving abilities.
Has a wide range of technical skills and operational knowledge.
Understands the practical applications to problems and situations ordinarily encountered.
Proficiency in operating Fluid Bed Dryers or equivalent.
Proficient in (Master Clean/Surface clean) equipment.
Proficient in setting up machinery.
Proficient in trouble shooting.
Ability to become a certified trainer and provide certified training in one process.
Ability to effectively interface with other departments if senior level (4th level) isn’t available.
Ability to participate in Continuous Improvement projects.
Qualified in both Weighing or Blending (where applicable) and at least in 1 of the following manufacturing processes: Granulation, Compression, Coating, Encapsulation, Potent Compound.
Observes safety and security procedures.
Determines appropriate action beyond guidelines.
Reports potentially unsafe conditions.
Uses equipment and materials properly.
Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.
Meets productivity standards; Completes work in timely manner; Strives to increase productivity; Works quickly.
Is consistently at work and on time; Arrives at meetings and appointments on time.
Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals. Completes tasks on time or notifies appropriate person with an alternate plan.
Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Able to build morale and group commitments to goals and objectives; Supports everyone's efforts to succeed.
Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information.
Speaks clearly and persuasively in positive or negative situations; listens and gets clarification; Responds well to questions; Demonstrates group presentations skills; Participates in meetings.
Comply with all Company policies and procedures.

Responsibilities

Operates pharmaceutical production machinery and follows the procedures for manufacturing such as weighing, blending, dispensing, mixing, coating, encapsulating, granulating, drying, milling, blending, compressing.
Meets requirements for use of manufacturing equipment and other commonly used equipment per SOP’s.
Executes written SOP’s to ensure the purity of materials involved in the manufacturing process.
Properly uses all scales, including printouts, zeroing, setting tares, and daily calibration verification per SOP’s.
Examines manufacturer Product ID Labels, Quality Control release tags, and Batch Production Record to verify issued/staged raw materials can be released for production.
Cleans manufacturing equipment and facilities according to established SOPs.
Executes machine change-overs from batch to batch.
Completes a variety of assignments independently based on established procedures.
Identifies process improvements that drive increased efficiency, throughput and quality.
Samples batches, including validation batches, for quality testing.
Executes required in-process product quality checks and documents accurately.
With Master Clean/Surface Clean certification, releases room to be master and/or surface cleaned.
Understands and runs processes to meet the assigned schedule and standards/routers; when this is not achieved, participates in the debrief to understand the reasons why and what needs to be corrected moving forward.
Completes documentation associated with manufacturing processes (e.g. batch record and logbooks) with detail and accuracy.
Meets requirements for entries on all applicable Batch Production pages, completion and attachment of all dispensary and weight verification tickets.
Verifies the manufacturing process on BPR in an accurate and timely manner.
Provides status updates and operational challenges on status boards.
Proactively identifies and troubleshoots process issues and, as a team member, analyzes root causes and makes recommendations.
Typically participates in Continuous Improvement projects of a higher scope & complexity.
Carries out processing/manufacturing activities safely, as required, on a daily basis.
Follows all safety and compliance procedures and participates in required training.
Adheres to all cGMP compliance/regulatory mandates and quality requirements.
Participates in safety teams, start-up discussions, incident debriefs, etc.
Ensures compliance with SOPs, Policies and Procedures as required by Company and regulatory agencies.
Maintains a clean, organized work area.
Conforms to all training requirements, including company required and machine specific training.
May become a certified trainer and provide mentoring and training.
Exhibits teamwork and motivates others to achieve project objectives.
Collaborates within own work unit and with those from other departments outside of work unit and/or with external vendors/suppliers.