Manufacturing Assembler II

Rani Therapeutics Inc.; Fremont (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

Rani Therapeutics Inc. in Fremont, CA is looking for a Manufacturing Assembler II to assemble parts for high-quality medical devices, requiring advanced assembly skills and strict adherence to GMP/GDP.

The role emphasizes precision, reading procedures in English, and contributing to team goals while adhering to schedules. On-site work and strong documentation practices are essential.

Qualifications

• 1–2 years in medical device or pharmaceutical manufacturing.
• Proficiency with basic arithmetic and measurements.
• Experience with GMP and GDP practices preferred.
• Ability to read and follow English procedures.

Responsibilities

• Assemble parts and components at one station with precision.
• Ensure GMP and GDP compliance in all tasks.
• Record hours and maintain legible documentation.
• Follow written procedures and safety practices.
• Assist in developing and updating assembly procedures.
• Identify problems and recommend corrective actions.

Skills

Advanced assembly skills

Attention to detail

Mechanical aptitude

Basic arithmetic

English communication

Education

High School Diploma or equivalent

Medical Device GMP certification

Tools

Microsoft Excel

Microsoft Word

Job description

Department: Manufacturing

Reports to: Production Supervisor

Position Overview

The Manufacturing Assembler II is responsible for assembling parts and components used in the production of high-quality medical devices. This position requires advanced assembly skills, attention to detail, and a strong understanding of manufacturing practices. The role involves adhering to industry standards and regulations, ensuring that products meet quality specifications and are assembled with precision.

Key Responsibilities

• Perform assembly operations requiring fine hand dexterity and precision.


• Proficiently assemble at least one assembly station or line, ensuring efficient and accurate production.


• Ensure compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) in all tasks.


• Adhere to work schedules and accurately report hours worked.


• Maintain legible and accurate records, including initialing, dating, and making clear notes.


• Follow all written procedures and safety practices to ensure a safe working environment.


• Read, comprehend, and follow written procedures and instructions in English.


• Assist in the development, revision, and maintenance of assembly procedures, protocols, and checklists.


• Identify and evaluate problems during assembly, make initial recommendations for corrective actions, and escalate issues as needed.

Experience

• 1 – 2 years of experience in a Medical Device or Pharmaceutical manufacturing environment.


• Proficiency in basic arithmetic and measurements.


• Strong mechanical aptitude is required.


• Prior experience in the medical device industry is preferred.


• Ability to effectively collaborate within a team and contribute to achieving team goals.


• Flexible and adaptable, with the ability to navigate uncertain situations.


• Proven proficiency in using Microsoft Excel and Microsoft Word.

Education

• High School Diploma or equivalent.


• Strong written and verbal communication skills in English.


• Relevant certification related to the position (e.g., Medical Device Manufacturing certification, GMP certification) is a plus.

Physical Demands

• The employee is regularly required to stand, walk, and sit for extended periods during the performance of job duties.


• Must be able to physically be present on-site to perform the required tasks.