Operator I
Chipton-Ross
Job Description
Job #218517 Chipton-Ross is seeking an Operator I for a contract opportunity in Skaneateles, NY. BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE) To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Ability to Read and Understand Instructions:
Tyler Harrell View phone number on click.appcast.io
View email address on click.appcast.io
Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.
Job #218517 Chipton-Ross is seeking an Operator I for a contract opportunity in Skaneateles, NY. BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE) To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Ability to Read and Understand Instructions:
- Candidates must be able to read and comprehend job instructions, part specifications, and assembly drawings. This skill is crucial for following detailed assembly processes accurately.
- The ability to visually detect defects in components and finished products is essential. This includes attention to detail to ensure quality standards are met.
- The ability to work effectively as part of a team and communicate clearly with colleagues, team leaders and supervisors is vital in a collaborative assembly environment.
- Entry-level assemblers should possess basic problem-solving skills to address minor issues that may arise during the assembly process.
- Candidates should be willing to learn and adapt to new processes, station changes, technologies, and changes in production requirements in a fast-paced environment.
- Assemble and test, as applicable, medical devices, equipment, and components according to established procedures and quality standards.
- Review quality points with the work instructions to meet quality standards.
- May use hand tools, automated machinery, and power tools to complete assembly tasks in compliance with GMP and FDA regulations.
- May assemble electronic components and modules according to detailed schematics, diagrams, and instructions, ensuring compliance with quality standards and specifications.
- May complete Device History Record (DHR) paperwork per unit, ensuring accurate documentation of production activities based on station assigned, and if included in work instruction.
- Prepare and organize kits with the necessary components and materials for assembly processes.
- Verify the accuracy and completeness of kit contents to ensure all required components are included following the work instructions provided.
- Maintain inventory levels of kit components and replenish as needed.
- Label and package kits for distribution to assembly lines or other departments.
- Handle materials, parts and assemblies, ensuring they are properly stored following guidelines provided.
- Maintain accurate inventory levels of components by following work instructions for replenishing any materials needed to complete production of assigned station.
- Reporting any discrepancies or quality issues to Team Leaders.
- Escalate any quality issues of parts, materials, defects or non-conformities to a team leader.
- Follow all SOP and work instructions to ensure they meet quality specifications.
- Ensure compliance with regulatory requirements and internal standards, documenting all activities in accordance with the client policies and procedures.
- Complete all required training programs and certifications within designated timeframes.
- Participate in lean manufacturing initiatives to improve efficiency and productivity.
- Package and label component parts or assemblies for shipment per the work instructions, ensuring protection from potential shipment damage and that all vital parts and instructions are present.
- Adjust or stack boxes on pallets to prepare for shipping or storage based on work instructions and SOP in compliance with safety standards.
- Proactively contributes to zero harm in the workplace for all employees by complying with legal and corporate (EHS) Environmental Health & Safety requirements, safe work practices, and EHS policies and procedures consistently.
- Maintain a clean and organized workspace, adhering to 6S principles and company standards.
- Report all hazards, near misses and incidents as soon as practicable and participate in identifying actions to prevent harm from occurring to our people and/or our environment.
- Employees at every level are responsible for quality (GMP) Good Manufacturing Processes and regulatory performance in the department to ensure quality program is met.
- Ensure compliance with government regulations, legal documents and safety & ethical standards as outlined by the client policies & procedures.
- Assemble and test, as applicable, medical devices, equipment, and components according to established procedures and quality standards.
- Review quality points with the work instructions to meet quality standards.
- May use hand tools, automated machinery, and power tools to complete assembly tasks in compliance with GMP and FDA regulations.
- May assemble electronic components and modules according to detailed schematics, diagrams, and instructions, ensuring compliance with quality standards and specifications.
- May complete Device History Record (DHR) paperwork per unit, ensuring accurate documentation of production activities based on station assigned, and if included in work instruction.
- Prepare and organize kits with the necessary components and materials for assembly processes.
- Verify the accuracy and completeness of kit contents to ensure all required components are included following the work instructions provided.
- Maintain inventory levels of kit components and replenish as needed.
- Label and package kits for distribution to assembly lines or other departments.
- Handle materials, parts and assemblies, ensuring they are properly stored following guidelines provided.
- Maintain accurate inventory levels of components by following work instructions for replenishing any materials needed to complete production of assigned station.
- Reporting any discrepancies or quality issues to Team Leaders.
- Escalate any quality issues of parts, materials, defects or non-conformities to a team leader.
- Follow all SOP and work instructions to ensure they meet quality specifications.
- Ensure compliance with regulatory requirements and internal standards, documenting all activities in accordance with the client policies and procedures.
- Complete all required training programs and certifications within designated timeframes.
- Participate in lean manufacturing initiatives to improve efficiency and productivity.
- Package and label component parts or assemblies for shipment per the work instructions, ensuring protection from potential shipment damage and that all vital parts and instructions are present.
- Adjust or stack boxes on pallets to prepare for shipping or storage based on work instructions and SOP in compliance with safety standards.
- Proactively contributes to zero harm in the workplace for all employees by complying with legal and corporate (EHS) Environmental Health & Safety requirements, safe work practices, and EHS policies and procedures consistently.
- Maintain a clean and organized workspace, adhering to 6S principles and company standards.
- Report all hazards, near misses and incidents as soon as practicable and participate in identifying actions to prevent harm from occurring to our people and/or our environment.
- Employees at every level are responsible for quality (GMP) Good Manufacturing Processes and regulatory performance in the department to ensure quality program is met.
- Ensure compliance with government regulations, legal documents and safety & ethical standards as outlined by the client policies & procedures.
- Prolonged Standing: The role requires standing for extended periods, often for the entire duration of the shift (up to 8 - 12 hours depending on assigned station and shift).
- Walking: Frequent walking within the production area to move between workstations, retrieve materials, and transport finished products.
- The role may involve lifting and carrying materials or components, typically up to 25-55 pounds, depending on the specific assembly tasks. This includes moving items boxed items from storage areas to the assembly line and vice versa.
- Team lift or lifting equipment required for over 40 lbs. following our clients ergonomics policy.
- Frequent lifting and carrying of lighter items (typically under 25 pounds)
- Accredited High School Diploma or GED.
- Full-Time- Monday- Friday- 06:30am-03:00pm
- Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
- Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.
Tyler Harrell View phone number on click.appcast.io
View email address on click.appcast.io
Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.
Vacancy posted 16 hours ago
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