Pharmaceutical Production TeamLead Technician, 3rd Shift (S-TH, 11p-730a)-Hikma Pharmaceuticals

Job Description

Job Title: Pharmaceutical Production TeamLead Technician, 3rd Shift (S-TH, 11p-730a)

Company: Hikma Pharmaceuticals

Location: Columbus, OH

Pay: $22.75 per hour

AI Pay Analysis: The hourly rate of $22.75 for a “Pharmaceutical Production Team Lead Technician, 3rd Shift” in Columbus, OH, appears to be somewhat below the industry standard for similar roles in the pharmaceutical manufacturing sector. Typically, Team Lead positions in this field can command rates ranging from $25 to $35 per hour, depending on experience, specific responsibilities, and local market conditions. Columbus’s cost of living and regional wages for technical roles also support a higher compensation benchmark. Thus, while $22.75 may be within a reasonable range for entry-level positions, it may not be competitive for a leadership role, especially considering the responsibilities typically associated with a Team Lead position in pharmaceutical production.

Job description:
We are seeking a highly skilled and motivated Production Lead Technician to join our dynamic team. In this role, you will leverage your advanced operational and process knowledge to enhance team performance. You will operate equipment, allocate resources, and provide training and mentorship to fellow technicians. Additionally, you will communicate production status across shifts to ensure adherence to cGMP, FDA, DEA, OSHA, and other relevant regulations.

As a Production Lead Technician, you will take an active role in Performance Center meetings, driving continuous improvement initiatives. You will monitor and oversee line and area performance concerning key performance indicators (KPIs) and engage your team in identifying safety hazards, influencing corrective actions, and modeling a safety-first mindset.

Your responsibilities will include manufacturing and packaging products in accordance with established policies, procedures, and regulatory guidelines while ensuring that all documentation—both written and electronic—is accurate and complete. You will be responsible for setting up and operating equipment in your designated area, verifying that all materials, products, and equipment are correct and approved for use. Quality will be a top priority, and you will halt production should any quality concerns arise, addressing issues promptly to minimize idle time.

Key Responsibilities:
– Ensure regular and predictable onsite attendance and punctuality.
– Maintain qualifications and proficiency in equipment setup, operation, and cleaning.
– Complete batch documentation accurately and review others’ documentation to ensure compliance with policies and regulatory guidelines.
– Execute disassembly and cleaning processes to maintain high standards.
– Address atypical situations by referencing appropriate work instructions and standard operating procedures, escalating issues as necessary.
– Engage proactively in identifying and addressing safety hazards.
– Participate in safety audits, ensuring risks are identified and resolved through the Area Ownership Program.
– Ensure materials used are properly documented in batch records and Enterprise Resource Planning (ERP) systems.
– Drive discussions related to quality and compliance, focusing on root cause analysis and corrective actions.
– Collaborate with Maintenance and Supervisory teams to ensure prompt maintenance and equipment reliability.
– Maintain performance boards to support operational consistency and standardization.
– Facilitate effective communication and performance monitoring across shifts.
– Act as a training subject matter expert, educating and mentoring fellow technicians.
– Support the onboarding of new employees and cultivate a positive team culture.

Qualifications:
– High school diploma or GED.
– Relevant experience in a manufacturing environment, with familiarity in documentation, setup, operation, cleaning, and basic maintenance of manufacturing equipment.
– Proficient in data entry and maintenance in SAP or equivalent systems.

Preferred Qualifications:
– Experience in the pharmaceutical sector or other regulated environments (cGMP).
– At least 18 months of experience in pharmaceutical manufacturing or packaging.

Hikma Pharmaceuticals USA Inc. is committed to diversity and inclusion and welcomes applications from candidates across all backgrounds. We strive to provide a comprehensive benefits package and a culture where safety and quality are organizational priorities. If you possess the necessary qualifications and are ready to make a meaningful impact, we encourage you to apply.

Job Posting Date: Thu, 05 Dec 2024 06:11:30 GMT

Apply now!