Job Purpose
The Senior Associate-Intellectual Property and Technical Writing will be responsible for drafting and review ofdocuments/reports pertaining to IP related to development, preclinical, Chemistry, Manufacturing and Controls (CMC) of Ocugen’s early stage, clinical and commercial products. This position reports directly to Manager, Medical and Scientific Writer and will play both a strategic and tactical role within Ocugen’s R&D team.
Duties & Responsibilities
Working Conditions
This position operates in an office setting and may include 20% of travel.
Physical Requirements
This is a largely sedentary role
Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past,
current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.
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